IQVIA

Job OverviewDirect and manage the execution of the strategic, operational and financial delivery of required Site Activation activities, including but not limited to Site ID and Selection, Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company, scope of work and/or sponsor requirements. Essential Functions• Provides strategic planning and project oversight accelerating Site Activation through best in class project management to ensure fast site activation for patient enrollment, responsibilities may include;  Accountable for multiple regions.• Support and/or participate in pre-award/bid defense activities.• Oversee the execution of Start Up (including pre-award through Site Activation) and/or Lifecycle Maintenance for assigned projects in accordance with the agreed start up strategy, adhering to agreed project timelines and in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol, customer requirements, and internal policies.• Study Delivery Scope minimum expectations: accountable for multiple regions or Global SAM project oversight responsibilities.• Develop, implement and maintain the Site Activation Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.• Collaborate with key stakeholders both internal and external, through effective communication and resolution management, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the Site Activation Management Plan.• Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents.• Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.• Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations. Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the Site Activation Management Plan.• Provide ongoing updates and reporting to various levels of the organization, both study team and in some cases senior level colleagues.• Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.• Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.• Adhere to quality standards, regulated and Company specific through the duration of the trial period.• Mentor and coach colleagues as required: mentor to Grade 140.• May take a lead role in developing long standing relationships with preferred IQVIA customers:Maintain and develop the customer relationship through study teamwork and support providing input to customer level processes and/or initiatives , attend Early Engagement Customer or Partnership Meetings if required.• Deliver presentations/training to clients, colleagues and professional bodies, as required.• Contribute to initiatives that affect positive change within the department and organization: support department and organizational initiatives. Qualifications• Bachelor's Degree Life sciences or related field• At least 5 years with 2 years of lead experience in a scientific or clinical environment.• Demonstrable experience in an international role; or equivalent combination of education, training and experience. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.• Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.• Prepare site regulatory documents, reviewing for completeness and accuracy.• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.• Review and provide feedback to management on site performance metrics.• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.• Inform team members of completion of regulatory and contractual documents for individual sites.• Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.• Perform quality control of documents provided by sites.• May have direct contact with sponsors on specific initiatives. Qualifications• 1 year clinical research experience. Equivalent combination of education, training and experience.  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree.• Some organizations require completion of CRA training program or prior monitoring experience.• Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewDirect and manage the execution of the strategic, operational and financial delivery of required Site Activation activities, including but not limited to Site ID and Selection, Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company, scope of work and/or sponsor requirements. Essential Functions• Provides strategic planning and project oversight accelerating Site Activation through best in class project management to ensure fast site activation for patient enrollment.• Support and/or participate in pre-award/bid defense activities.• Oversee the execution of Start Up (including pre-award through Site Activation) and/or Lifecycle Maintenance for assigned projects in accordance with the agreed start up strategy, adhering to agreed project timelines and in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol, customer requirements, and internal policies.• Study Delivery Scope minimum expectations: accountable for 1 region with multiple countries.;• Develop, implement and maintain the Site Activation Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.• Collaborate with key stakeholders both internal and external, through effective communication and resolution management, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the Site Activation Management Plan.• Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents.• Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.• Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations; identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the Site Activation Management Plan.• Provide ongoing updates and reporting to various levels of the organization, both study team and in some cases senior level colleagues.• Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.• Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.• Adhere to quality standards, regulated and Company specific through the duration of the trial period.• May take a lead role in developing long standing relationships with preferred IQVIA customers: maintain and develop the customer relationship through work at the study team level.• Deliver presentations/training to clients, colleagues and professional bodies, as required.• Contribute to initiatives that affect positive change within the department and organization: support department initiatives. Qualifications• Bachelor's Degree Life Science or related field.• At least 3 years relevant experience in a scientific or clinical environment.• Demonstrable experience in an international role; or equivalent combination of education, training and experience.• In-depth knowledge of clinical systems, procedures, and corporate standards• Strong knowledge of medical terminology and regulations• Broad knowledge of clinical research• Strong knowledge of Microsoft Office and e-mail applications• Effective communication, organizational, and interpersonal skills• Ability to work independently and to effectively prioritize tasks• Ability to delegate effectively• Ability to manage multiple projects• Attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作。 对所负责的研究中心进行方案和研究相关的培训，与研究中心进行定期沟通以管理项目进行中的要求和问题。 评估研究中心工作的质量和完整性，确定研究中心是否是按照方案和适用的法规进行研究。将质量问题汇报给负责的PM和/或直线经理。 通过追踪注册申报和批复、招募和入选、病例报告表（CRF）完成和递交、以及数据疑问产生和解决的情况，管理所负责研究中心的进展。创建和维护与研究中心管理、监查访视的发现以及行动计划相关的文件，递交访视报告和其他所需研究文件。 负责相应研究中心的研究财务管理。 与其他职能部门共同合作。 完成直线经理和/或项目经理（PM）分配的其他工作。IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

OverviewIQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. IQVIA has two teams focused exclusively on amplifying the patient’s voice and enhancing their experiences across their health journey: the Patient-Centered Solutions and Connected Technologies (PACT) team, and the Instrument Licensing Solutions and Patient and Site Strategy (ILS & PASS) team. These teams work closely together to generate patient experience data (PED) through clinical outcome assessments (COAs; including digital health technologies), qualitative research, and patient preference research. The ILS & PASS team has a small group dedicated to thought leadership and COA instrument development. This “science team” is focused on (a) ensuring that sound scientific principles permeate through the research completed by the PACT and ILS & PASS teams, and (b) leading the development, validation, and qualification of COA instruments to collect reliable and interpretable data from patients in medicines development and routine clinical care. The ILS & PASS science team comprises dedicated qualitative scientists and COA development scientists. Presently it does not have a team of dedicated statisticians and psychometricians. Owing to the large body of work – mostly internally funded – the team is recruiting for a Statistics and Psychometrics Lead, one entry-level Statisticians/Psychometrician, and one Statistical Programmer to support the teams’ activities, as described below. The Statistician/Psychometrician and Statistical Programmer roles will report to the Statistics and Psychometrics Lead. The Statistical Programmer role is described below. Role & Responsibilities The Statistical Programmer will be expected to: (1) Empirically develop scoring rules & program scoring algorithms for existing COA measures For instruments being added to IQVIA ILS library, generate standard scoring documentation, and program simulation datasets, Data Quality Evaluation (DQE), and scoring of domains on these datasets Implement new statistical features in the random generation of data, to simulate real-world instrument data with certain psychometric properties Implement new, more advanced statistical capabilities in user tools (Insights Hub, PROCore) Work cross-functionally with non-statisticians/psychometricians in the PACT and ILS & PASS teams (2) Provide programming support for the development of new COA measures & endpoints Program classical and modern psychometric analyses and analyses of meaningful thresholds Program high frequency and continuous DHT data collaborate with data scientists to support algorithm validation, and verification of digital measure performance across diverse datasets and devices. About You Knowledge, skills and abilities Candidates must have: (a) statistical and psychometric research skills; and (b) strong computer skills, including Base SAS with macro (R skills, API experience). Connecting to databases with SAS/R, and programming with validation/QC in a regulated environment would be an advantage. Candidates should demonstrate: (a) excellent written and oral communication skills including grammatical/technical writing skills; (b) critical attention and accuracy with details; and (c) strong individual initiative, organizing skills, and commitment to quality. Candidates must be able to: (a) work within a team environment, and to establish and maintain effective working relationships; (b) confidently communicate with, and effectively present information to, internal and external teams; and (c) work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks and projects. Candidates should have extensive familiarity and demonstrable experience with AI tools and their application to the topics mentioned above. Education and experience Candidates should have a relevant qualification in statistics or psychometrics, experience in statistical programming, and an interest in patient-centered research (including COA and/or DHT) and clinical research (pharmaceutical, or healthcare industry). Consulting experience with pharmaceutical companies is desirable. This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Internal Job DescriptionRole DescriptionWe are seeking an experienced Senior Data Engineer to join our AI team. In this role, you will lead the development and optimization of data infrastructure supporting our Agentic AI initiatives. You will collaborate with ML engineers, AI scientists, and product managers to architect, implement, and maintain robust data pipelines powering autonomous AI agents. As a senior member of the R&DS AI Innovation Program, you will help shape data strategy and ensure our data solutions scale to meet the demanding requirements of next‑generation AI systems. Key ResponsibilitiesMandatoryDesign, develop, and maintain scalable data pipelines and ETL processes supporting AI research and development. Design and maintain scalable data models (e.g., star schemas, feature‑ready datasets, semantic layers) for analytics, ML training, and agent workflows. Collaborate with AI scientists and engineers to gather data requirements and ensure availability and quality. Implement data governance and security measures to protect sensitive information. Establish observability, lineage tracking, and monitoring frameworks to detect anomalies, freshness issues, and operational failures. Implement data partitioning, indexing, and storage optimization techniques for large‑scale AI datasets. Monitor and troubleshoot data pipeline issues to ensure continuity and reliability. Stay current with emerging data engineering and AI technologies. Drive data platform reliability, scalability, and cost optimization across cloud‑based infrastructure. PreferredDesign and implement scalable, resilient data architectures for AI agent training, fine‑tuning, and inference workflows. Build streaming and event‑driven pipelines enabling real‑time agent feedback, telemetry, and adaptive learning. Develop and maintain high‑performance pipelines using modern orchestration frameworks to support real‑time agent interactions. Create specialized storage and retrieval systems for vector embeddings, knowledge graphs, and symbolic reasoning components. Implement automated data validation, schema testing, and quality checks ensuring reliable AI training datasets. Implement comprehensive monitoring and governance frameworks ensuring high‑quality training data and compliance with privacy regulations. Continuously optimize system performance with a focus on reducing latency for agent decision‑making. QualificationsEducation Bachelor’s or Master’s degree in Computer Science, Data Engineering, or a related field; advanced degree preferred. Experience 5+ years of professional experience in data engineering, including at least 2 years focused on ML/AI data infrastructure. Programming & TechnologiesAdvanced proficiency in Python and Scala; experience with Rust, Go, Java, or Julia is valued. Expert‑level knowledge of SQL and NoSQL databases. Hands‑on experience with vector databases (e.g., Pinecone, Weaviate, Milvus). Proficiency with modern data orchestration platforms (e.g., Airflow 2.x). Cloud & InfrastructureExtensive experience with at least one major cloud platform (AWS, Azure, or GCP). Expertise in containerization and orchestration (Docker, Kubernetes). Experience with Infrastructure as Code tooling (e.g., Terraform). Data ProcessingExperience with distributed computing frameworks (Spark, Dask, Ray). Proficiency with streaming technologies (Kafka, Flink). Knowledge of modern data lakehouse architectures. Preferred QualificationsCertifications in cloud platforms, big data technologies, engineering, or ML operations. Experience collaborating with ML engineers on CI/CD pipelines for data processing and model deployment. Working knowledge of ML frameworks (PyTorch, TensorFlow). Experience with feature stores and experiment‑tracking platforms. Understanding of LLM fine‑tuning data requirements and processing. Experience developing data systems for autonomous AI agents or agentic AI applications. Background in prompt engineering or retrieval‑augmented generation systems. Experience with semantic caching and efficient storage/retrieval of AI‑generated artifacts. Familiarity with LLM evaluation metrics and benchmarking frameworks. Expertise in hybrid architectures combining traditional databases with vector stores. Experience with RAG systems and related data pipelines. Knowledge of RLHF data workflows. Experience mentoring junior engineers, establishing best practices, and contributing to architectural decisions. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan and database deliverables to internal and external customers. Provide technical advice and solutions with internal and external customers to solve problems and improve efficiency. Ensure that staff is trained and compliant with current operating procedures and work instructions and project scope of work. Identify and address professional development/training needs of staff. Mentor staff members to develop Data Management process, system, and drug development expertise. Provide operational input into proposals and scope of work. Participate in proposal defenses. • Hold at least bi-monthly meetings with direct reports to discuss, at a minimum: project status, including timelines, delivery updates, financial aspects of the group or project, and potential risks, associated mitigation and support required; status of any initiatives that they may be involved in; the team's utilization rates; the direct report's training and other administrative obligations, such as Standard Operating Procedures (SOPs) and corporate training mandates; personnel issues; and career or training objectives. • Develop and implement plans for measuring and improving employee engagement, ensuring global consistency.• Collaborate with project leads to address work scheduling for current and projected projects, staffing needs, technological needs, and projected peak workloads, ensuring global consistency, where possible. Develop and manage associated action plans to hold members accountable. • Efficiently conveying messages from leadership to direct reports and teams, as well as effectively communicating issues and opportunities up to leadership. • Might be needed to serve as the designated substitute or alternatively ensure coverage is in place for direct reports during their absence or in case of turnover. • Attend and participate in Bid Defenses, Kick off Meetings (KOM), as applicable. Support Request for Information (RFI), Request for Pricing (RFP), and budgets, as requested. • Participate / Support internal and external audits and inspections, as required. Also ensure required staff is assigned, trained and prepared to support. Technical Skills:Experience on clinical data management.Experience working on TA like Oncology.Extensively work on rave EDC tool. Educational Qualification:• Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req • Equivalent combination of education, training and experience in lieu of degree. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Spanish Bilingual Site Research Assistant – Aventura, FLWork Setup: On-siteScheduled Hours: 40 hours per weekAbout IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.Job SummaryThe Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements. This position requires strong attention to detail, the ability to prioritize in a fast‑paced environment, and excellent communication skills. Experience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued.Key ResponsibilitiesPerform EDC data entry and query resolution in a timely and accurate manner.Review patient charts and records from the site database to support protocol‑required tasks.Build and maintain strong working relationships with investigators, clinical staff, and study teams.Assist in screening, prescreening referrals, recruiting, and enrolling research participants.Manage scheduling of participants, visit scheduling, reminders, and protocol‑related procedures.Collect participant history and coordinate laboratory requirements and follow‑up care.Support the informed consent process, ensuring adherence to IRB‑approved protocols.Promote participant safety by following protocol guidelines and reporting requirements.Ensure compliance with Sponsor and company SOPs, policies, and regulatory guidelines.Maintain study supplies and support upkeep of the regulatory binder.Record (but not obtain) vital signs as required by study protocol.QualificationsMinimum of an associate’s degree or equivalent combination of education and experience.At least 1 year of experience in a clinical research setting (preferred).Working knowledge of clinical trials, GCP principles, and study‑specific procedures.Familiarity with cardiovascular studies (preferred).Demonstrated experience with:Reviewing charts from site databasesPrescreening referralsEDC entry and query resolutionVisit scheduling and remindersMaintaining study suppliesUpkeep of regulatory bindersRecording (not obtaining) vital signsAbility to perform required clinical procedures and understand medical terminology.High attention to detail and strong organizational skills.Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders.Certifications and licenses as required by company, state, country, or regulatory bodies.Spanish Bilingual is requiredNote: This position is not eligible for sponsorship.#LI-CES #LI-DNP #LI-HCP #ONSITEIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

 The team & the company   IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. IQVIA RWS is a fast-growing and highly successful consultancy business, focusing upon on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry.   Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 200 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, biochemistry, and epidemiology, based in 12 geographies, with projects delivered across >50 countries.  Our clients operate in the life sciences industry, including global top 20 pharmaceutical companies, medical device, and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.  For more information about our company please visit our website: https://www.iqvia.com/  Role purpose  This role will offer you the opportunity to support our EMEA Health Economics team as a Consultant Medical Writer and be part of our HTA Evidence & Strategy Centre of Excellence and Value Communications Centre of Excellence.  This role focusses on medical writing for HEOR purposes, where you will be responsible for writing tasks within HEOR projects and work with a senior team to co-manage small workstreams, project tasks and thought leadership initiatives. Typical projects include medical writing for the new EU Joint Clinical Assessment (JCA) dossier, HTA dossiers (e.g., NICE, SMC, NCPE, etc), global value dossiers, protocols and reports for literature reviews, reports for evidence synthesis and health economic modelling studies, and HEOR-focused peer-review manuscripts and conference abstracts. The audience for the project deliverables will be various life-sciences customers as well as healthcare payers, providers, and regulators. You will work within a team of highly experienced health economists and outcomes research specialists providing support across a range of HEOR projects, working in a cross-functional and cross-country project team, providing medical writing, undertaking quality control, and contributing to the management of project delivery (including guiding the work of more junior team members). The role will expose the candidate to the broad range of EMEA RWS offerings in value communications, HTA strategy and HEOR to support in business development opportunities. An ideal candidate will have a good understanding of the matrix structure typical of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve clients’ aims, as well as proven success in communicating scientific information in a strategic way to optimize a product’s access to markets and reimbursement.   Qualifications and Skills  Previous experience with medical writing is essential for the role. We are looking for proactive individuals with strong analytical and problem-solving skills. Candidates should have a strategic mindset, the ability to identify potential issues and suggest solutions. The ideal applicant should have apt interpersonal skills and the ability to establish relationships with both internal team members and clients. As such, fluency in conversational and business English is essential. The ability to demonstrate this through slide deck development, report writing, and presentations is essential.  We recruit individuals from a variety of backgrounds to join our well-rounded team. If you are motivated, have a passion for healthcare, and strong organisational skills and experience in medical writing we encourage you to apply. The list below should be viewed as a guide rather than a checklist.  Degree in life sciences (or related), epidemiology or health economics and policy, preferably a Master’s degree;  Significant experience in medical writing, including being the primary writer on peer-reviewed publications and HEOR study reports/protocols;  Familiarity with health economics and health technology assessment is a benefit;  Strong written and verbal English communication skills, expertise in scientific writing requirements;   Excellent Microsoft office skills (expert in use of MS Word), and high attention to detail;   Self-motivated with a strong desire to learn quickly and independently, ability to work autonomously with appropriate guidance when needed;  Strong time-management and organisational skills, and flexibility to work in a fast-paced environment;  Interest in data visualisation and presentation;  Keen to work as a member of a diverse, multi-cultural team.  Responsibilities   Write high-quality HEOR study reports and protocols, HTA/GVD dossiers, manuscripts, conference abstracts;  Work with senior team to co-manage small workstreams, project tasks and thought leadership initiatives;  Conduct quality control reviews of HEOR documents and maintaining audit trails of changes;  Mentor and train less experienced Medical Writers;   Contribute to medical writing training initiatives to upskill the team and set quality standards;  Support the team’s Centre of Excellence initiatives.   Please submit your CV in English. Please note that we're not able to sponsor visa for this position. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Team  IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients.      Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 90 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, epidemiology and data management, located across 8 geographies.   Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. Our clients look for insight and evidence on the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.    For more information about our company please visit our website: https://www.iqvia.com     Role overview  In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The role of the Consultant is expected to play an important role in shaping the team’s literature review offerings.   The successful candidate:  Will be involved in shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team  Has a good understanding of systematic literature methods (e.g., Cochrane)  Can independently develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, PubMed, etc.) and proficient in using OVID SP or another similar platform  Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews and be an in-house go-to expert for the team  Has a good understand of different types of literature reviews (e.g., systematic, targeted, pragmatic, etc.)  Manages literature review projects with senior oversight  Guides the team on interpretation/qualitative synthesis of the literature review findings   Oversees literature review projects that meet rigorous HTA requirements, conducts quality control of literature review deliverables (searches, screening files, extractions, reporting)  Is a day-to-day contact with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters based in the EMEA region, and occasionally their affiliate teams, with senior oversight  Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols   Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches   Collaborates with other business areas and functions of the organisation to deliver client services and support the development of new offerings  Qualifications and desired experience We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. The ideal candidate will also have a good understanding of the typical structure of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client’s aims.   The list below should be viewed as a guide rather than a checklist. We want to prioritise recruiting candidates who will incorporate IQVIA’s value of ‘brave minds’ with their previous experience to put a personal spin on this role. If you share our passion for driving healthcare advancements through unparalleled data and have a passion for collaboration and solving complex problems, we encourage interested candidates who feel like they could be a good fit for the role to apply.  Desired skills and qualifications:   Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science  Prior relevant experience, >2 years (such as, but not limited to experience in systematic literature reviews and/or meta-analyses)  Understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs  Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research   Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis  Excellent oral and written communication skills  Accuracy, attention to detail and time management skills  An understanding of meta-analysis methods is advantageous, but not essential  Strong written and verbal communication skills with fluency in English  Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous   Proficiency in MS Word, PowerPoint, Excel  Eligibility to work in one of our office locations without visa sponsorship   Please submit your  CV in English. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry dedicated to creating intelligent connections that deliver unique innovations and actionable insights. We help to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access and delivery of healthcare, and ultimately drive better health outcomes. With approximately 90,000 employees, IQVIA conducts operations in more than 100 countries. We are currently looking for an Associate Director, Brand Outsourcing Strategy and Offering Development to join IQVIA! Commercial Brand Outsourcing represents a significant share of sales across launch and established brand portfolios of pharmaceutical companies that can be deprioritized, with potential revenue and profit growth remaining untapped. In this key role, you will be responsible for supporting the Brand Outsourcing Offering within the Global Commercial Solutions business unit, reporting to the Global Head of Commercial Brand Outsourcing. It will have three key elements: offering strategy and development, sales enablement (including some client engagement), and operational alignment. You will coordinate with stakeholders across global and local business units, working with regional teams to identify and execute growth opportunities. The role will be high-profile and dynamic. Essential Functions Leads the hunt for new assets, acquisitions, and/or partner channels to accelerate portfolio expansion and market potential. Drives the development of complete offerings (from I&A through C&S). Ensures offering content and feature levels are competitive and sufficient to generate targeted revenue growth and market penetration. Makes offering lifecycle decisions necessary to deliver business results (including sunset or extension decisions). Incorporates IQVIA strategic direction into offering management decisions within and across business lines. Recognized as the spokesperson for IQVIA on its offerings both internally and externally. Secures organizational agreement on the complete go-to-market plan and budget required for implementation. Manages cross-functional teams to ensure the offerings meet customer needs and are economically and technically viable and deliverable. Approves research plans to ensure outputs fulfill research objectives and coaches others on market analytics best practices. Endorses conclusions and uses recommendations from market analytics to make business and planning decisions. Brings external thought leadership to bear in the client environment. Recognizes the impact of industry developments that may influence IQVIA products, services, or trends. Forecasts trends, identifies potential impacts, and applies knowledge to offering development and business line strategy. Drives achievement of objectives for an increasingly larger or more complex area of business line responsibility (or multiple smaller areas) and ensures execution of plans. Proactively shapes and scopes interdependencies with other business line stakeholders and functions to achieve business line goals. Determines and executes plans for recovery, contingency, and mitigation to address market, corporate, or other impacts. Leverages, builds, and maintains IQVIA relationships that contribute to successful execution of plans. Proactively engages and manages stakeholders, leads interdependent teams, and demonstrates complete ownership of the business. Key Responsibilities Portfolio Strategy & Innovation Support the development and evolution of the global BO offering, ensuring it meets client needs and aligns with IQVIA’s broader commercial strategy to drive more technology-, data-, and AI-enabled offerings. Act as a solution and subject matter expert for internal clients to support business development teams, including throughout RFIs and RFPs. Coordinate with regional teams to identify, assess, and activate opportunities for Brand Outsourcing services, leveraging local insights and capabilities. Manage key internal and external stakeholders, fostering alignment, engagement, and accountability across functions and geographies. GTM enablement Enhance BO offering awareness by actively engaging with account teams and regional/local BD stakeholders to communicate the BO offering. Support the marketing team in the preparation of BO-specific and targeted promotional materials/activities (webinars, articles, etc.) to drive internal and external awareness of the IQVIA offering. Lead regular internal BD/account team meetings to share client and market demands and tailor the core outsourcing offering to different needs. Support the development of pricing and commercial models for different client segments. Lead/support BO pipeline tracking and expansion, with regular pipeline reviews across all markets (regional calls and bi-weekly sales calls). Proactively identify opportunities using insights and data for internal teams to leverage in client discussions. Support RFP/RFI processes as an SME, sharing best practices and experience from other global deals. Support new and existing BO projects with data-driven analytics and consulting insights. Organizational Alignment & Operating Model Share best practices, proposal innovation, and commercial learnings across all markets. Lead and deliver the global RBU pipeline cadence, including, for example, aligning product codes. Support the development of compliance, quality, and governance processes. ​Qualifications & Experience Bachelor’s degree or equivalent required; advanced degree preferred. 7+ years of relevant experience in pharmaceutical, biopharma, healthcare services, or agency environments, including experience in marketing, sales, or commercial roles, with at least 4 years in senior management or leadership positions. Proven experience in offering development, portfolio management, and/or go-to-market (GTM) strategy. Demonstrable track record in managing portfolio brands and driving offering or commercial strategy. Strong understanding of pharmaceutical commercial models, brand strategy, and outsourcing solutions. Experience supporting business development activities, including RFPs, RFIs, and pipeline development. Strong stakeholder management experience across global and regional teams. Strategic mindset with the ability to translate industry trends, including data, technology, and AI, into actionable plans. Strong strategic business and industry awareness. Excellent communication, interpersonal, and stakeholder engagement skills. Strong analytical, problem-solving, organizational, and project management capabilities. Strong team player with the ability to work creatively in a fast-paced environment, managing changing priorities and demanding timelines. Ability to work effectively in a fast-paced, matrixed, global environment. Commercial acumen with a focus on revenue growth and client value creation. Proficiency in MS Office and general digital tools; knowledge of IQVIA offerings, systems, or similar environments is preferred. Strong organizational, planning, and logistics skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Senior Data Engineer – Kazakhstan (Remote) About the Role We're growing our technology footprint in Kazakhstan and looking for a Senior Data Engineer to join our expanding regional team. You'll design, build, and deliver modern data solutions that power our operations across Eurasia and support global business initiatives. You'll work with a modern data stack — Azure, Databricks, Python, Scala, Spark — and collaborate daily with international engineering teams on large-scale, high-impact data platforms. As a senior member of the team, you'll bring technical leadership, mentor others, and help shape best practices. The role is fully remote, open to candidates anywhere in Kazakhstan. This is a hands-on senior data engineering role focused on building robust, scalable data pipelines and platforms. It does not include user support or helpdesk responsibilities. What You'll Do Design and develop complex data solutions that meet defined functional and technical requirements.Architect, build, and maintain data pipelines on Azure and Databricks, supporting both batch and large-scale processing workloads.Lead the migration of regional data systems to global Azure-based platforms.Troubleshoot and optimize complex data workflows, improve performance, and maintain clean, sustainable code.Define and apply advanced data quality and testing standards across the team.Review code, refactor legacy modules, and optimize SQL and cloud-based queries.Lead medium-to-large scale data engineering initiatives within the team.Mentor and onboard new engineers, and actively contribute to knowledge sharing and technical guidance.What We're Looking For Education Bachelor's degree in Computer Science, Software Engineering, Data Engineering, or a related technical field.Must-Have Technical Skills Programming Python (primary language) — strong, production-level proficiencyScala (Spark-level proficiency)Cloud & Big Data Microsoft AzureAzure Databricks — clusters, jobs, SQL warehouses, environments, and cost monitoringApache Spark for large-scale data processingDatabases MS SQL or equivalent relational database experienceStrong SQL skills for data transformation and query optimizationExperience & Languages 5+ years of hands-on commercial data engineering experience, including a track record of delivering production-grade data solutions.Proven, real-world experience with Azure + Databricks in previous senior roles.Experience mentoring engineers and leading technical initiatives.Fluent English — required for daily interaction with global teams.What We Offer A chance to join a fast-growing Kazakhstan hub delivering on global initiatives.Work with modern cloud technologies and scalable data platforms.Fully remote role, open to candidates from any region in Kazakhstan.Collaborative culture with access to global expertise, training, and technical mentorship.Competitive compensation aligned with the local market.About the Team Our data engineering team supports production systems across the CIS and Eurasia region and is now fully transitioning to global Azure-based components. You'll join a technically strong, internationally connected team building data solutions used around the world. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Country Manager – Nigeria Region Covered: West Africa (Primary focus: Nigeria)Business Unit: Molecular / Diagnostics Contracted with IQVIA Role Overview We are seeking an experienced and commercially driven Country Manager to lead and grow our Molecular Diagnostics business in Nigeria, one of Africa’s most complex and strategically important healthcare markets. This role carries full commercial, operational, and people leadership responsibility, with a strong emphasis on public and private sector growth, deep engagement with local healthcare funding mechanisms, and long-term sustainability. The successful candidate will bring strong industry experience, established relationships within the Nigerian healthcare ecosystem, and a proven ability to develop and execute country‑specific sales and market access strategies. Key Responsibilities Commercial & Strategic Leadership Partner closely with the Managing Director to define, develop, and execute a Nigeria‑specific strategy to profitably grow the Molecular Diagnostics business across public and private sectors.Define and implement long-range strategic plans, ensuring alignment with regional and global priorities.Establish comprehensive sales strategies and execute all tactical initiatives required to achieve revenue, profitability, and market share objectives.Hold full P&L responsibility, including forecasting, target achievement, and performance tracking.Prepare, present, and manage annual business plans, with regular performance updates.Ensure all activities are conducted in a legal, ethical, and compliant manner, in line with regulatory requirements.Sales Excellence & Operational Management Lead, coach, and manage a team of Sales Executives and Ambassadors, driving execution excellence and sustained performance.Own and execute sales plans to achieve revenue growth, improved profitability, higher win‑rates, and increased share of wallet.Propose and manage human and financial resource allocation to maximize productivity.Monitor and control budgets and expenditure against approved allocations.Support the field team with contract negotiations, particularly around pricing and profitability.Act as a trusted advisor and senior contact for key customers.Oversee customer issue escalation through to resolution, ensuring high levels of customer satisfaction.Ensure effective use of salesforce management systems, KPIs, incentive plans, and performance management tools.Government, Funders & Market Access Build and maintain strong working relationships with:Federal and State Ministries of HealthGovernment agencies and regulatory bodiesPublic health laboratories and reference laboratoriesLocal and international laboratory funders and donorsDemonstrate a strong understanding of Nigeria’s healthcare funding mechanisms, procurement structures, and reimbursement models.Navigate tender processes, donor-funded programs, and public health initiatives effectively.Position the organization as a strategic long-term partner within the Nigerian healthcare system.Customer & KOL Engagement Establish and execute structured Key Opinion Leader (KOL) engagement plans, in collaboration with Marketing.Maintain regular engagement with top KOLs, laboratory directors, and C‑suite stakeholders.Implement mechanisms to monitor the effectiveness of KOL engagement.Maintain a strong understanding of market dynamics, competitive landscape, pricing, and reimbursement challenges.Translate market insights into actionable commercial strategies.People Leadership & Talent Development Develop, motivate, and challenge teams to achieve high performance and accountability.Identify and develop high‑potential (HIPO) talent, with clear development and succession plans.Build leadership capability through active coaching and mentoring.Drive appropriate recognition, rewards, and engagement initiatives.Foster a collaborative, ethical, and results-driven culture.Required Knowledge & Experience Minimum 6 years’ experience in a senior commercial or country leadership role.At least 3–4 years’ proven people management experience.Strong commercial background within healthcare, preferably IVD, Diagnostics, Molecular, or related markets.Demonstrated experience in the Nigerian market, including understanding of:Public healthcare systemsLaboratory funding and donor mechanismsGovernment and regulatory engagementEstablished relationships with KOLs, laboratories, and healthcare stakeholders are a strong advantage.Proven ability to develop and execute country-specific sales strategies.Strong leadership, negotiation, financial analysis, and communication skills.Ability to influence and operate effectively within a matrix organization.Qualifications University degree in Medical Technology, Biochemistry, Biomedical Sciences, or a related field.Understanding of Molecular Diagnostics sales processes is highly advantageous.Strong business planning, project management, and analytical capabilities.High level of accountability, agility, and the ability to manage multiple priorities.French language skills are an advantage, particularly for regional collaboration and West African engagement.Experience in finance or strong analytical skills will be considered a plus.Why Join Us This role offers a unique opportunity to lead a high-impact diagnostics business in Nigeria, shape national strategy, influence key healthcare stakeholders, and build teams that drive sustainable growth while improving patient access to advanced diagnostics. #LI-DNP #LI-CES  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Role DescriptionWe are seeking an Engineering Manager / Delivery Lead to own end‑to‑end delivery execution for Agentic AI solutions within AI & Technology Solutions (ATS), Clinical AI & Technology Innovation (CAITI). This role is accountable for translating product intent and architectural direction into reliable, compliant, high‑quality delivery outcomes, by leading internal teams and external vendors. Operating as part of the Core Development Team, the Engineering Manager is the single point of accountability for delivery execution, owning sprint cadence, SDLC deliverables, delivery readiness, and release orchestration from Proof of Concept through Production. This role works in tight partnership with: AI Product Manager & Product Owner (value, scope, priorities)AI Solution Architect & Tech Lead (architecture, patterns, technical direction)Program Manager (governance, cross‑program alignment, escalation)while retaining clear decision authority over delivery execution. Key Responsibilities Own end‑to‑end delivery execution for Agentic AI solutions from Proof of Concept through Production, ensuring predictable, high‑quality outcomes.Translate product scope and architectural direction into clear delivery plans, sprint cadence, and execution milestones.Drive day‑to‑day engineering delivery, including dependency management, issue resolution, and removal of execution blockers.Ensure delivery readiness across environments, CI/CD, quality gates, validation, and release governance.Coordinate and orchestrate internal teams and vendors to deliver as a single, integrated delivery unit.Partner closely with Product, Architecture, QA, Validation, and Program Management to ensure delivery aligns with regulatory, quality, and governance expectations.Provide transparent delivery reporting, proactively surface risks, and escalate issues with clear options and trade‑offs.Support release and rollout execution (pilot to scale) and ensure effective handover to operations.Lead and mentor a multidisciplinary engineering team (AI engineers, data engineers, platform engineers), providing technical guidance, career development, and performance management.Act as delivery owner for vendor‑contributed work, including: 1) Task integration, 2) Quality expectations, 3) Delivery timelines.Ensure vendor outputs meet IQVIA standards and are integrated seamlessly into CI/CD and release processes.Surface delivery risks related to vendor dependency early and clearly.Key Qualifications Experience 7+ years in engineering delivery roles, with demonstrated ownership of end‑to‑end delivery in complex systems.Proven experience delivering Agentic AI, AI‑enabled, or data‑intensive platforms, including systems that incorporate reasoning, orchestration, retrieval, or automation components.Experience delivering AI solutions in regulated or highly governed enterprise environments, with accountability for production readiness, auditability, and lifecycle controls.Demonstrated ability to coordinate cross‑functional teams and external vendors delivering agent‑based solutions across prototype, MVP, and production stages.Technical & Delivery Background Bachelor’s degree with 10+ years of experience, or Master’s degree with 7+ years of experience in Computer Science, Information Systems, or a related technical field.Strong understanding of Agentic SDLC / ADLC concepts, including agent lifecycle management, phased progression.Experience delivering systems that require agent evaluation, monitoring, and feedback loops, including performance, reliability, and behavioral drift considerations.Ability to engage credibly with Solution Architects, Tech Leads, and AI teams on agent feasibility, orchestration complexity, dependency sequencing, and delivery risk.Practical understanding of CI/CD for agentic systems, including environment readiness, controlled releases, rollback strategies, and post‑deployment monitoring.Proficiency in programming languages such as Python, Java, or Scala, with strong understanding of data structures and algorithms.Scala, with strong understanding of data structures and algorithms.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 217 300,00 zł - 461 700,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

AI Full Stack Software Engineer (Agentic AI & UI Focus)Role DescriptionWe are seeking a mid-level AI Full Stack Software Engineer to join our AI team. In this role, you will design, build, and enhance intelligent applications supporting our Agentic AI initiatives. You will work across frontend, backend, and AI integration layers, partnering closely with ML engineers, AI scientists, product managers, and architects to deliver user-facing AI solutions. As part of the R&DS AI Innovation Program, you will contribute to secure, scalable, and production-ready applications that enable autonomous and semi-autonomous AI agents, while growing toward broader technical ownership. Key ResponsibilitiesMandatoryDesign, develop, and maintain full stack applications supporting AI research, prototyping, and production use cases.Build modern, responsive, and intuitive user interfaces using React and JavaScript for AI-driven workflows and dashboards.Develop robust backend services and APIs using Python and Java to support agent orchestration, business logic, and system integration.Design and implement microservices-based architectures for scalable and maintainable AI applications.Collaborate with AI scientists, engineers, and product managers to translate business and technical requirements into user-facing applications.Integrate AI applications with enterprise systems, APIs, databases, and cloud platforms.Apply software engineering best practices including testing, observability, documentation, and automation.Ensure security, compliance, auditability, and protection of sensitive data in application design and development.Troubleshoot and resolve frontend, backend, integration, and performance issues across the application stack.PreferredContribute to application architectures supporting agent workflows, including orchestration layers, tool integrations, and human-in-the-loop experiences.Build and enhance applications supporting near real-time agent interactions and feedback loops.Develop UI patterns for conversational interfaces, workflow dashboards, and agent action visibility.Support integration with vector stores, retrieval systems, or knowledge-based AI components.Assist with performance optimization to reduce latency in agent-driven workflows.Contribute to deployment automation and environment setup using modern DevOps practices.Work with cross-functional teams to define reusable frontend and backend patterns for AI products.QualificationsEducationBachelor’s degree in Computer Science or a related field.ExperienceTypically 3+ years of professional experience in software engineering or full stack application development.Programming & TechnologiesStrong proficiency in Python, React, JavaScript, and Java.Experience building frontend/UI applications with a focus on usability and responsiveness.Experience developing backend APIs, services, and microservices.Familiarity with modern software engineering practices, including testing, debugging, and version control.Cloud & PlatformsHands-on experience with at least one major cloud platform (AWS, Azure, or GCP).Experience with CI/CD practices and deployment workflows for modern applications.Familiarity with API integrations, databases, and distributed system design.Preferred QualificationsFamiliarity with LLM-based applications, agentic frameworks, or AI workflow orchestration.Experience with containerization and orchestration tools such as Docker and Kubernetes.Exposure to RAG-based architectures, retrieval systems, or AI application monitoring.Understanding of secure development practices in enterprise or regulated environments.Experience building user-facing tools for analytics, operations, or AI-assisted decision support.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 134 100,00 zł - 248 900,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Intern, Site Activation Coordinator Join IQVIA today and make an impact on patients’ outcomes! Job Overview Provide administrative and technical support to ensure efficient preparation, handling, and maintenance of essential clinical trial documentation and activities. Support site activation, regulatory processes, and ongoing trial management in accordance with study protocols, applicable regulations, and internal procedures. Due to the nature of the tasks—which are focused on handling physical clinical trial documentation—this is a fully office‑based role located in Warsaw (Domaniewska Street). This is a fixed‑term internship with an 8‑month employment contract, offering an excellent first step into the clinical trials industry and a valuable opportunity to gain hands‑on experience. Responsibilities Supporting printing, compilation, and shipment of clinical trial documentation required for site activation, study maintenance, and regulatory submissions for selected studies or multi‑protocol programs in Poland.Assisting in the preparation, distribution, filing, and archiving of trial documentation according to the scope of work and standard operating procedures (SOPs).Reviewing documents for completeness, consistency, and accuracy under the guidance of senior staff.Preparing client‑facing deliverables using appropriate tools and drafting text for straightforward documents as assigned.Completing and updating relevant fields in Clinical Trial Management Systems (CTMS), databases, tracking tools, timelines, and project plans.Providing administrative support including meeting coordination, minute taking, travel arrangements, copying, scanning, faxing, and courier management.Interacting professionally with internal and external clients under supervision of senior team members.Performing investigational product (IP) release activities for small, straightforward projects or providing support for reviews within larger programs.Qualifications Completed Bachelor’s Degree in a relevant field.Fluent written and verbal communication skills in Polish and English.Demonstrated analytical, critical‑thinking, and problem‑solving ability.Proficiency with standard office software and willingness to learn role‑specific tools.Strong teamwork skills and the ability to collaborate effectively with colleagues and stakeholders.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 57 700,00 zł - 102 300,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

【ポジション名】Senior Consultant / Manager～Associate Principal(Management Consulting) 【会社紹介・ビジョン】私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。 【部署・チーム名】Management Consulting（コンサルティング部門） 【所属部署・チーム概要】Management Consultingは、IQVIAの戦略コンサルティング部門として、ヘルスケア・ライフサイエンス業界の変革テーマを専門に扱うチームです。 クライアント：製薬企業を中心に、医療機器メーカー、コンシューマーヘルス企業、投資ファンドなど多岐にわたる対応領域：革新的新薬の研究開発からコマーシャライゼーションまでの各フェーズにおける戦略立案組織最適化、営業改革、業務プロセス改善AI含むソリューション構想策定・実装全社戦略、成長戦略、事業ポートフォリオ戦略、M&A/LA、海外進出/日本参入戦略社内テクノロジーチームとの協業によるデジタルテーマ（業務改革の構想・実装）強み：ライフサイエンス領域における深い専門性を有し、IQVIA国内外のデータプラットフォーム・デジタルアセット・専門人材を活用しながらクライアントの課題解決を支援【チームの雰囲気】コンサルファーム、ITベンダー、投資ファンド、製薬企業、医療機関など多様なバックグラウンドのメンバーで構成オープンでニュートラルな雰囲気で、専門性を活かした議論が活発グローバルプロジェクトも複数常時進行しており、世界レベルでの課題感やベストプラクティスを共有できる環境新薬・デジタルヘルスなど新しいテーマが多く、常に新たな学びや成長機会が豊富挑戦を歓迎し、成長を重視するカルチャー【ポジション概要・チームが目指すゴール】本ポジションは、ライフサイエンス領域の戦略プロジェクトの中心人物として、クライアントの最重要課題を解決するための付加価値の高いソリューションを構想・実行します。APAC／グローバルチームと連携し、データ×戦略×テクノロジーを融合したコンサルティングを通じて、医療・ヘルスケア産業の変革をリードすることが求められます。 【主な業務内容】クライアントの課題解決に向けたコンサルティングプロジェクトの企画・提案・推進戦略テーマ（ブランド戦略、ローンチ戦略、NPP、デジタル戦略、営業組織改革等）のリードクライアント向けレポート・提案資料の作成および高品質なデリバリー新規ビジネス機会の創出（フォローオン案件、追加提案など）若手メンバーの育成・プロジェクトマネジメント業界動向を踏まえたインサイト提供社内外のステークホルダーとの連携・協業【役割への期待】若手メンバーをリードし、Project Managerとして高い品質でDeliveryする論理的思考力と分析力を発揮してクライアント価値を最大化する経営層との議論が可能なコミュニケーション能力を持つビジネス拡大に寄与する新規提案・機会創出への積極的な関与チーム全体の成長に資するリーダーシップ【求める人物像】（必須要件）コンサルティング会社または事業会社での戦略/企画/業務改善等の経験ライフサイエンス・ヘルスケア領域への強い興味や経験仮説構築力・論理的思考力・課題解決能力CEO/COO/CMOクラスを含む多様なステークホルダーと対話できる力プロジェクト推進力、チームワーク、若手育成への意欲日本語必須、英語ビジネスレベル歓迎【歓迎要件】製薬企業でのマーケティング／NPP／デジタル関連の経験マーケットアクセス、患者中心戦略の経験グローバル案件の経験Thought Leadership （講演・執筆等）データ分析・テクノロジーを用いたソリューション構築経験【このポジションの魅力・キャリアパス】ポートフォリオ戦略〜事業性評価〜営業戦略など、さまざまな切り口から企業成長に貢献できるAI/デジタル、グローバルアセットを活用した高インパクトの創出が可能コンサルパートナーだけでなく、事業会社マネジメント、スタートアップ、PEファンドなど多様なキャリアパスが描ける社会的インパクトの大きいヘルスケア産業の未来づくりに寄与できる【勤務地】東京（品川オフィス）／ハイブリッド勤務 【雇用形態・勤務時間・福利厚生・休日休暇】雇用形態：正社員勤務時間：9:00〜17:00フレックス勤務：あり在宅勤務制度：あり福利厚生：社会保険完備、IQVIA独自制度あり受動喫煙対策：あり休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇など試用期間：あり（通常6か月）【給与・待遇】当社規定により優遇昇給：あり賞与：あり時間外手当：あり【選考プロセス】書類選考 → 1〜3次面接 【応募方法】応募方法の詳細や連絡先については別途ご案内します。あなたのストーリーを、ぜひ聞かせてください。 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Sales Operations Analysts in the Go To Market Partnership Center are responsible for the operational support of internal Sales Teams, Account Managers & Principals to ensure successful Lead to Order opportunity management throughout the sales cadence process. This role calls for proactive, detail-focused professionals with exceptional communication skills, capable of engaging effectively across all levels of the organization. Ideal candidates thrive on solving complex problems, excel in fostering cross-team collaboration, and are driven to deliver impactful results. Essential Functions• Management of Salesforce (SFDC) opportunities from Pipeline to Close. Includes: Updating of Stages and Forecast Category, Adding/Updating of Products and Revenue Allocation, producing pricing support documents, and processing deals with finance.• Assisting in preparing templates for Statements of Work and initial Contract submissions.• Coordination of Professional Services Automation (PSA) platform. Includes: Coordinating Pricing Assistants for Resource Hours and Budgets, Creating Projects and Assigning Principals in Charge and Project Managers.• Attend pipeline calls/ team meetings with internal clients as requested and perform Salesforce and PSA updates post-call.• Cross functional Team coordination (Business Leads, Contracting, Finance, Sales, etc.) to ensure smooth processing of opportunities.• Continuous, pro-active coordination with internal client contacts and business personnel, to foster and maintain relationships.• Maintain the team’s document repository making sure information are up to date.• Accomplish other Ad-Hoc tasks, business initiatives and special projects as needed.• Help in strategic planning and analysis with Account Managers/PICs as needed.Qualifications• Bachelor's Degree• 2-3 years of experience in sales support and customer service• Finance/Sales Operations/Customer Relationship Management background is preferred• Strong Excel knowledge• Preferrable with experience of Microsoft 365 applications (Outlook, Teams, SharePoint, etc.)• SAP and SFDC or any other CRM system knowledge is a benefit• Strong team player and accepts coaching opportunities positively• Flexibility and willingness to join a dynamic and fast-paced working environment IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen.   Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können.   Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten.   Für ein internationales und forschendes Pharmaunternehmen suchen wir zum nächstmöglichen Zeitpunkt einen Pharmareferenten im Bereich gynäkologische Onkologie (m/w/d) als Customer Partnering Manager. Im Gebiet: Stuttgart-Reutlingen Das sind Deine Aufgaben: Als Customer Partnering Manager bist Du der Regisseur für regionale Strategien und sorgst dafür, dass Lösungen genau dort ankommen, wo sie gebraucht werden. Patient Journey Navigator: Du analysierst Hürden in der Diagnose und Behandlung und leitest daraus mutige Handlungsoptionen ab. Wissenschaftlicher Partner: Du berätst medizinisches Fachpersonal auf Augenhöhe und stellst eine transparente, rechtmäßige Anwendung von Produkten sicher. Event-Gestalter: Du planst und moderierst Fortbildungsveranstaltungen sowie wissenschaftliche Produktschulungen, um Wissen direkt erlebbar zu machen. Beziehungs-Architekt: Du bist der primäre Ansprechpartner für Deine Stakeholder und baust ein starkes, crossfunktionales Netzwerk auf. Impulsgeber: Du bringst Markt-Trends proaktiv ins Team ein und gestaltest die Disease Area Strategie aktiv mit. Das bringst Du mit: Du hast ein abgeschlossenes Studium (Medizin, Naturwissenschaften oder BWL) Du bringst Erfahrung aus der Pharmaindustrie mit Du erfüllst die Voraussetzungen als Pharmaberater:in nach AMG Du denkst unternehmerisch, triffst Entscheidungen auf Basis von Mehrwert und sprichst fließend Deutsch und Englisch Du besitzt Wissen im Bereich der Onkologie sowie Kenntnisse der Gesundheitsregulatorik Der Umgang mit digitalen Kommunikationstools (z.B. Zoom, Google Suite) ist für Dich so natürlich wie das Atmen Du denkst unternehmerisch, triffst Entscheidungen auf Basis von Mehrwert und sprichst fließend Deutsch und Englisch Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Onkologie #Gynäkologie #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Are you passionate about improving healthcare and making a real difference in the lives of stroke patients? Join IQVIA as a Junior MSL and be part of a global effort to enhance stroke care. This role offers a unique opportunity to work in a dynamic and international environment, partnering with a leading global pharmaceutical company dedicated to innovative healthcare solutions. If you are motivated, scientifically driven, and ready to travel across Bulgaria to support hospitals and healthcare professionals, we want to hear from you! Territory:  BulgariaTravel: Up to 70% Ideal Location: Sofia   About Us:Every 30 minutes, a stroke patient who could have been saved dies or is permanently disabled because they were treated in the wrong hospital. Our mission is to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all existing stroke centers. We are building a global community of stroke centers and stroke-ready hospitals, working every day to improve the quality of treatment for every stroke patient.   RESPONSIBILITIES: As a Junior MSL, you will: Increase efficiency in the management of stroke patients, support hospitals, EMS, and healthcare professionals with continuous training and organizational tools, promote new diagnostic and treatment guidelines to hospitals as an expert Therapeutic Consultant, promote quality monitoring programs to ensure consistent performance of hospitals and EMS, extend the reach of the project to new hospitals, lead multidisciplinary stroke teams through continuous improvement, improve therapeutic protocols in major hospitals. REQUIRED SKILLS: Strong scientific background – ideally PhD in Neuroscience, high motivation with strong interpersonal and stakeholder engagement skills, fluency in English and Bulgarian, flexible, solution-oriented with problem-solving skills, accountability and ownership, resilient and able to operate effectively in fast-paced environments, experience in the healthcare environment, including work with healthcare organizations and healthcare professionals, actively seeks opportunities to improve processes and outcomes, valid driving license; experienced driver, availability to travel up to 70% of the time, eligibility to work full time in Bulgaria. #LI-CES #LI-VK1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Mitarbeiter IT-Support (m/w/d) Standort Singen (Vollzeit) Die IQVIA Commercial GmbH ist Teil der IQVIA-Unternehmensgruppe und Spezialist maßgeschneiderter Softwarelösungen zur Integration in bestehende Systeme speziell für den Gesundheitsmarkt sowie für die Pharma- und Druckindustrie. Werden Sie Teil unseres Entwicklungsteams und arbeiten im spannenden und innovativen Umfeld. Deine Aufgaben: Eigenverantwortliche Installation und Inbetriebnahme der Softwarelösungen zur Qualitätskontrolle bei Endkunden Betreuung von Kunden aus der Druck- und Pharmaindustrie Schulung der Anwender in der Bedienung der Software Durchführung von Soft- und Hardwaresupport Support per Telefon, Remote-Service-Tools sowie direkt vor Ort beim Kunden Dein Profil: Abgeschlossene technische Ausbildung, z. B. in Drucktechnik, Mechatronik, Elektrotechnik oder einem vergleichbaren Bereich Kenntnisse in Netzwerkstrukturen sowie Client- und Server-Betriebssystemen von Vorteil Grundkenntnisse im Bereich Datenbanken wünschenswert Kenntnisse in der Softwarevalidierung von Vorteil Aufgeschlossene Persönlichkeit mit Freude an der Zusammenarbeit im eigenverantwortlichen Team Selbstständige, strukturierte Arbeitsweise und Bereitschaft, sich neuen Herausforderungen zu stellen Hohe Kundenorientierung sowie Flexibilität und Reisebereitschaft im In- und Ausland Gültiger Führerschein der Klasse B Verhandlungssichere Deutschkenntnisse (mind. C1) sowie gute Englischkenntnisse (mind. B2) in Wort und Schrift Worauf Du dich freuen kannst:  Flexible Arbeitszeitmodelle Willkommen in unserem Team mit individuellen Entwicklungsmöglichkeiten Ein sehr gutes Arbeitsumfeld mit flachen Hierarchien, wertschätzendem Umgang und hoher Kollegialität Strukturierte Einarbeitung und Wissenstransfer Vielseitige Tätigkeit in einem dynamischen IT-Unternehmen mit Weiterbildungsmöglichkeiten Neue offene Büroflächen in super Lage in Singen am Bodensee mit vielen Freizeitmöglichkeiten Rabatte über IQVIA Corporate Benefits Ladesäulen für Elektrofahrzeuge IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Business Unit: Global Site Activation Location: UK, homebased, occasional travel to office Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: You will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessaryReview documents for completeness, consistency, and accuracy, under guidance of senior staffPrepare site documents and inform team members of the completion of regulatory contractual documentsDistribute completed documents to sites and internal project team membersUpdate and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific informationReview, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documentsRequirements: Bachelor’s Degree in Life Science or related field1 - 3 years’ prior experience in Life Sciences or similar (or equivalent combination of education, training and clinical, healthcare and/or pharma experience)Ability to work independently but also collaborate with othersJoin IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic AreasBe part of a global team who operate across 141 locationsExposure across a variety of studies and projectsAccess to new, innovative technologiesWork within a collaborative and vibrant environmentOwn your career!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewDesigns/develops software solutions requiring general domain knowledge and developing business experience.Analyzes user requirements/needs and makes decisions within limited parameters under regular supervision. Essential Functions• Designs/develops software solutions requiring general domain knowledge and specialized business experience.• Works at all layers of the application stack including front-end user interface and backend development.• Analyzes user requirements/needs and makes decisions within general parameters under regular supervision.• Supports and often lead projects within own organization with limited complexity, including the development of medium size system components.• Has strong and broad understanding of quality standards and work requires minimal revision.• Reviews complex functional specifications and other validation deliverables as assigned.• Provides peer support and helps on-board new Software Engineers to the team. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req Or• 3 to 5 years prior related experience in developing web applications, graduate experience, or demonstrated success in development with DrugDev Spark or equivalent system Req• Experience with Ruby on Rails, Python, React, Ember or similar web framework.• Ability to write clean code• History of successfully designing small to medium system components• Good interpersonal communication and presentation skills• Attention to detail• Technical/functional expertise• Communication• Decision making• Customer focus• Conflict management• Energy, motivation and work rate IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.