IQVIA

About the Team: At IQVIA, our Patient Centered Solutions (PCS) team is dedicated to integrating the patient voice into medical research and development. Our scientific consulting services group conducts qualitative, quantitative, and mixed methods studies to better understand the patient, clinician, or caregiver experience. Projects range in size, type, and across multiple disease areas, and include clinical outcome assessment (COA) development, modification, and validation to support medical product development; strategic consulting for regulatory needs; exploratory analyses of existing data; literature review and gap analysis; and non-interventional studies with conceptualization, primary data collection via qualitative and/or quantitative methods, analysis, interpretation/synthesis, and dissemination phases. You'll enjoy a rewarding career in a collaborative, multicultural environment that values growth and development. Role Overview: Join IQVIA as a Manager and play a key role in executing and delivering on primary literature reviews, data collection efforts, and analysis/reporting of qualitative and/or quantitative data. Your expertise will support customers in life science and population health markets with patient reported outcome (PRO) and other COA solutions, and will directly influence the success of clinical trials and patient-centered, observational studies. In this role, you will be responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. You will also identify and elevate potential new business opportunities and assist in the business development and proposal process. You will also receive the training, mentorship, and additional experience needed to advance in a research career track. Key Responsibilities: Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects, leveraging primarily qualitative or mixed-methods approaches. Reviews and analyzes client requirements or problems and assists in the development of proposals of cost-effective solutions that ensure profitability and high client satisfaction. Provides direction and guidance to Consultants, and where relevant, to Statistical Services assigned to engagement on overall project objectives, client needs, and scientific execution of the project with assistance from subject matter experts (SMEs). Develops or oversees development of detailed documentation and specifications, including protocol and study document development. Performs or oversees qualitative analyses to assist in the reporting of studies to address client needs and the development of client specific solutions. Supports the design, structuring, and delivery of client reports and presentations that are appropriate to the characteristics or needs of the audience. Act as primary contact for clients on a project; may also deliver some findings to clients. Recommends improvements and alternative solutions to resolve problems on projects to address client needs. May identify new business opportunities of follow-on work and new leads at assigned client. Provides follow-up with client after project deliverable has been completed to ensure client satisfaction. Proactively develops broader and deeper knowledge of related consulting and life sciences research methodologies through on-the-job experience and participation in training and mentorship opportunities. Begins to develop specific subject matter expertise to support Centers of Excellence or other specialty groups within PCS. When acting as Project Manager, proactively manages project timelines, project finances, and manages day-to-day communication with the client and team members. Qualifications: Educational and Professional Experience: Master’s or doctorate degree in the social sciences or life sciences. 5–8 years of consulting experience managing and delivering COA (mainly PRO) selection, creation, and validation projects for pharmaceutical or life sciences clients. Professional Skills: Solid project management skills and client relationship building skills. Works willingly and effectively with others in and across the organization to accomplish team goals. Ability to manage multiple projects, juggle priorities, and deliver on tight deadlines. Knowledge of key issues and current developments in the life science industry, particularly around qualitative and mixed-methods approaches to COA development and validation. Excellent presentation and communication skills. Some subject matter expertise to effectively manage projects. Technical Skills: Experience in qualitative research methods and literature review methods required. Additional survey research and mixed-methods or quantitative research methods experience preferred. Proficient in MS Office (Word, Excel, PowerPoint); experience with bibliographic software, such as Zotero; experience with qualitative coding software, such as MAXQDA. Language and Travel: Fluency in English and no travel requirements (with occasional travel for conferences or client meetings possible). 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, when annualized, is $95,700.00 - $239,200.00. 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.

Job OverviewManage medium to large multi-regional Connected Devices projects that are stand-alone or full-service in scope, across all clinical trial phases.  Ensure all project work is completed to the sponsor's satisfaction, on time and within budget and in accordance with policies and procedures. Essential Functions• Plan, initiate, execute, control, and deliver projects in accordance with the Scope of Work agreed with the customer.• Serve as the primary contact for a given Sponsor to ensure communication is maintained and reporting schedules are adhered to.• Drive resource planning and support the project team to ensure adequate resourcing of the project throughout its life cycle, referring to senior management for advice as appropriate.• Lead the Connected Devices cross-functional teams to ensure successful delivery of assigned projects.• Track and supervise project progress, identify and evaluate project risks, and take corrective action as appropriate.• Manage the project financials accurately and appropriately ensuring project goals are achieved according to customer’s expectations and within the scope of the project.  Ensure revenue recognition and forecasts are calculated accurately and change Orders executed where appropriate.• Ensure that all deliverables are of the expected quality standards and meet customer expectations and are per Connected Devices standard operating procedures.• Prepare and present project information at internal and external meetings.• Conduct an ‘End of Project’ review meeting to ensure that all project activities have been completed in full.• Keep Connected Devices leadership fully informed of any project issues that may impact quality, budget, and timeliness of project delivery to the customer’s satisfaction. Request support and advice for timely issue resolution as required.• Train and mentor new or junior project managers.• Provide input to line managers on project team members’ performance relative to project tasks to aid career development. Qualifications• Bachelor's Degree Life science or health care related discipline Pref• Five years related experience Required or equivalent combination of education, training and experience Required • Good leadership skills• Up to 20% travel• Good interpersonal and communication skills• Good problem solving skills• Excellent customer service skills• Good Microsoft Office 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 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, when annualized, is $79,300.00 - $198,200.00. 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.

Join IQVIA as a Senior Director, Nursing Services and play a pivotal role in advancing patient care, client partnerships, and innovative healthcare service delivery. This executive leadership opportunity is ideal for a dynamic leader who enjoys developing teams, building trusted client relationships, and leading large-scale nursing and patient support programs that make a meaningful difference in patients' lives. In this remote role, you will work with some of the industry's most recognized pharmaceutical and healthcare organizations, providing strategic leadership across complex nursing and patient engagement programs. The position offers significant executive visibility and opportunities to influence business strategy, service delivery, and client growth initiatives. Candidates must be willing to travel periodically for client meetings, business development activities, and leadership events, while maintaining flexibility to support clients and teams across varying time zones. If you are energized by solving complex challenges, leading through influence, and driving exceptional client outcomes, this is an opportunity to make a lasting impact within a growing and innovative organization. Job Overview As a Senior Director, Nursing Services, you will provide executive leadership for a portfolio of nursing and patient support programs. You will be accountable for client satisfaction, operational performance, strategic planning, and the development of leaders responsible for large field-based and virtual nursing teams. Working in a highly collaborative environment, you will partner with clients, internal stakeholders, and business development teams to ensure exceptional delivery of services while supporting future growth opportunities. This role requires strong consultative leadership and the ability to navigate complex stakeholder environments across healthcare and pharmaceutical organizations. Responsibilities include: Leading nursing-focused patient support and ambassador programs.Providing strategic oversight for large-scale healthcare service delivery operations.Building and maintaining executive client relationships.Serving as a senior escalation point for operational and client-related issues.Developing and mentoring directors and other operational leaders.Supporting business development activities and client solution discussions.Collaborating with technology, operations, and commercial teams to drive performance and innovation.Ensuring contractual commitments, quality standards, and financial objectives are achieved.Monitoring key operational and client success metrics.Leading organizations supporting approximately 100-250 employees through multiple management layers.Qualifications Bachelor's degree required; advanced degree preferred.10+ years of leadership experience within nursing services, patient support programs, healthcare operations, pharmaceutical services, or related healthcare environments.Experience managing complex healthcare programs and large operational teams.Strong client-facing leadership experience with demonstrated success managing executive stakeholder relationships.Proven ability to lead strategic initiatives and operational transformations.Experience supporting account growth, business development, and client retention activities.Strong financial, operational, and analytical skills.Excellent communication, problem-solving, and relationship-building abilities.Experience with patient engagement, field nursing, ambassador programs, or clinical support services preferred.Demonstrated ability to lead through influence in a matrixed 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 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, when annualized, is $116,600.00 - $324,800.00. 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.

Are you a strategic leader who thrives on building client partnerships, leading high-performing teams, and shaping the future of patient support services? IQVIA is seeking a Senior Director, Hub Services to lead a portfolio of complex patient support programs while driving operational excellence, client satisfaction, and business growth. This remote leadership role offers the opportunity to work with leading pharmaceutical manufacturers, influence critical healthcare programs, and collaborate with executive stakeholders across the industry. Candidates should be comfortable traveling periodically for client meetings, business reviews, and team engagement activities. Success in this role requires flexibility to support clients across multiple U.S. time zones and the ability to navigate a fast-paced environment where strategic thinking, relationship management, and problem-solving are equally important. As a key member of the leadership team, you will have a direct impact on patient access, client success, and the growth of IQVIA's patient support services business. Job Overview As a Senior Director, Hub Services, you will oversee a portfolio of client programs and serve as the executive leader responsible for ensuring successful delivery of contracted services. You will lead directors, associate directors, managers, and operational teams supporting patient and provider engagement across complex specialty and rare disease programs. This role requires a balance of strategic leadership, client relationship management, business development, and operational excellence. You will partner closely with internal stakeholders including technology, operations, finance, and business development teams to ensure client expectations are achieved while identifying opportunities for growth and expansion. Responsibilities include: Leading a portfolio of patient support and hub service programs.Managing and developing leaders responsible for large operational teams.Maintaining executive-level client relationships and serving as a key escalation point.Driving strategic account planning and portfolio growth initiatives.Supporting business development activities, including solution presentations and client meetings.Collaborating with cross-functional teams to optimize service delivery and performance.Monitoring operational, financial, and client satisfaction metrics.Ensuring delivery commitments and contractual obligations are achieved.Leading teams supporting approximately 100-250 employees through multiple levels of management.Qualifications Bachelor's degree required; advanced degree preferred.10+ years of progressive leadership experience within patient support services, healthcare services, specialty pharmacy, pharmaceutical services, healthcare operations, or related industries.Significant experience managing complex client relationships and large-scale service delivery operations.Demonstrated success leading leaders and managing large, multi-layered organizations.Strong business acumen with experience supporting sales, account growth, and business development initiatives.Experience overseeing operational performance, budgets, and client service metrics.Exceptional communication, presentation, and stakeholder management skills.Ability to navigate complex challenges, influence stakeholders, and drive organizational change.Expertise in patient support programs, hub services, reimbursement support, and healthcare service delivery preferred.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, when annualized, is $116,600.00 - $324,800.00. 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.

As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally.  Our teams help biopharma, medical device and diagnostic companies get their therapies to the people who need them.  We help customers gain insight and access to their markets and ultimately demonstrate their product’s value to payers, physicians and patients.  A significant part of our business is acting as the company’s sales force to physicians or providing nurses to educate patients or prescribers.  With the right experience, you can help deliver medical breakthroughs in the real world. IQVIA has the world’s largest Commercial Sales & Medical Solutions (CSMS) organization dedicated to the launch and marketing of pharmaceutical and medical products.  With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs. Job Summary: We are excited to announce we are looking for Nurses to support our Patient Support Program as a resource for patients living with acromegaly. Our nurses will provide education about specific disease treatments and resources to empower patients to understand and manage their disease state. Nurses are responsible for one on one communications with patients as well as medical professionals associated with the treatment process. Supervisory Responsibilities: Duties / Responsibilities: » Answers calls in a professional and timely manner. » Document review of prescriptions, case notes and appointment results. » Adverse Event review and reporting as necessary. » Initiate case creation in CRM. » Participate in scheduling process from start to finish by scheduling and confirming appointments with patients and network clinicians. » Assist in determining that each appointment is staffed with a properly credentialed clinician for the appointment location. » Document case details in Customer Relationship Management (CRM) system. » Place outbound calls and text messages to patients and network clinicians. » Answer incoming calls, text messages, and email correspondence. » Provide program coverage as needed when team members are out of office. » Escalate issues to leadership and work on Program improvements » Assist patients in finding resources for their disease state in their area » Educating patients on disease state » Coordinate and facilitate the connection between patients and program approved, patient-based resources. » Provide direct educational training to patients and assigned medication. » Provide patient-focused education to promote behavioral change for the empowerment of patients to improve specific treatment compliance » Foster appropriate dialogue between patient and health care provider Qualifications » Active Nursing License in good standing » Bilingual in English/Spanish required » Minimum of 2+ years of recent nursing experience that includes, but not limited to direct patient care, physical assessment, patient education, group in -servicing and proficiency in peripheral access. » Proven success utilizing good communication, speaking, and writing skills when interacting with customers. » Must be proficient with Microsoft Office, especially MS Teams, Excel, Word, and Outlook. » Experience with Salesforce, the Customer Relationship Management System (preferred). » Excellent time management skills and ability to multi-task and prioritize work. » Ability to interact courteously and professionally with patients and clinical staff. » Strong organizational skills with attention to detail. » Nurse educator experience preferred » Ability to work independently and as a team player. » Knowledge of clinical data and pharmacology » Demonstrated time management skills; planning and prioritization skills; ability to multi-task and maintain prioritization of key projects and deadlines » Travel up to 15%. Work Location: » Fully remote. #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 $90,000-$97,000 annually. 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.

Senior Global Trial Manager – Single Sponsor   Are you experienced in managing late phase clinical trials at a global level?   We are looking for a Senior Global Trial Manager to join our Single Sponsor Department. Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll lead critical aspects of global studies and collaborate across functions to drive success.   As part of your role, you’ll have the opportunity to specialise in one for the following areas: ·       Scientific Review Committee (SRC) ·       Non-Interventional Studies (NIS) ·       Managed Access Programs (MAP) ·       Investigator-Initiated Trials (IITs) ·       Research Collaborations (RCs) ·       Program Level Documents (PLD)   Key Responsibilities:   Clinical Documentation & Study Tools ·       Draft sections of protocols, CRFs, training materials, and data review plans ·       Contribute to the development of safety updates, IBs, and regulatory submissions   Project Leadership ·       Oversee data review and TMF audit readiness ·       Forecast/manage investigational product supply ·       Support study closeout, issue resolution, and lifecycle budget tracking ·       Contribute to Managed Access Program coordination and compliance   Vendor & Stakeholder Management ·       Coordinate CRO/vendor selection and performance ·       Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison ·       Lead cross-functional collaboration with data management, drug supply, and more   What You'll Bring ·       Advanced degree in life sciences or healthcare ·       2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials ·       Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports) ·       Excellent communication, organizational, and collaboration skills ·       Deep understanding of GCP and clinical trial design ·       Passion for advancing real-world evidence and patient outcomes Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. 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.

Responsibilities:•Provide hands-on administration and support for marketing automation platforms including Salesforce Marketing Cloud, Marketo, HubSpot and/or Pardot •Develop the day-to-day architecture of marketing automation platforms including MA instance(s) to enable campaigns & programs to run effectively (attribution, sourcing, lead flow)•Build & Execute lead lifecycle, lead scoring, nurture platforms, segmentation and data management initiatives •Assist in troubleshooting platform, campaign, and integration issues while identifying root causes and recommended resolutions.•Support client engagements by gathering requirements, documenting processes, and executing solutions aligned with business goals•Assist with CRM and marketing automation platform integrations to ensure data flows accurately between systems.•Build and maintain reports and dashboards to support campaign performance analysis and business objectives.•Identify and elevate products/solutions offered to meet current and future market needs by being familiar with technology stacks & major players in martech space (Adobe, Power BI/Tableau, etc…) •Contribute to internal process documentation and team knowledge-sharing initiatives.•Collaborative approach & effective communication: technical proficiency is a requirement but you must also be to process feedback, ask questions for additional detail, & explain technical elements to non-technical stakeholders•Manage and grow junior team members to both increase their soft skill development and their marketing automation acumen.•Support the creation of on-going training plans for internal teams including walkthroughs of client use cases, creation of frameworks, and how-to documentation. Helps Strategists identifythe need for client training and/or new processes and corresponding reference materials.• Support Strategists with strategy sessions and identifies other SMEs needed, supports the creation of discussion guides and assets for workshop meetings and helps recommend when/if these meetings are neededBase Qualifications:•B.S. or B.A. degree in marketing or analytics, or equivalent professional experience•5+ years of marketing automation experience desired•Experience working within Salesforce Marketing Cloud (SFMC)•Experience with Salesforce Sales Cloud or other CRM platforms preferred•Technical mastery of 1:1 platforms, specifically in advanced &/or admin capability (advanced program setup, lead scoring, customer lifecycle, data management)•Proven history of strategy development and technical problem-solving skills•Ability to think strategically with a strong ability to execute plans and exceed client expectations and project goals•Experience as an operations strategist, and/or owner of process and data management•Proven success in driving results-oriented marketing programs and strategies, and the ability to proactively identify opportunities for improvement and optimization•Must be able to speak to and demonstrate knowledge in the digital marketing field 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, when annualized, is $73,400.00 - $183,600.00. 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.

Our MedTech Clinical Educator RN experiences a unique opportunity and leverage your clinical expertise in a dynamic role that goes beyond bedside care. Collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology. You will be responsible for training and educating Registered Nurses on hospital beds within the Medical-Surgical unit. Job Responsibilities: Your primary focus will be in-servicing and education only; no sales responsibilities, and no bedside care. Provide peer-to-peer education and in-servicing to nurses, and hospital staff to support medical device implementations Assess customer-specific education needs and collaborate with staff to deliver a positive educational experience Utilize clinical nursing expertise to answer questions and address concerns with the medical device Provide updates, reports, and valuable feedback to client during and after in-service assignments Training for this role will be provided and is paid. You will have an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and learning the medical device industry.  Schedule: · Minimum availability of 2 weeks per month required. Required Qualifications: RN Degree - Associates required, Bachelor's preferred Active and Unrestricted RN license required Med-Surg/ICU/Acute Care experience of at least 1-2 years required Excellent communication skills Ability to clear hospital vendor credentialing requirements. Position may/will require up to date immunizations. Travel Requirement: Travel nationally to support customer needs. Driving is considered a business requirement for this role. Candidates must possess a valid driver’s license and will be subject to a review of their driving record prior to hire. Located within 1 hour of a major airport. Travel, and your time traveling is paid. Preferred Qualifications: Med Surg, ICU, Critical Care or Acute Care experience of at least 2-3 years is preferred Leadership experience (manager, educator, preceptor) can be helpful but is not required Ability to learn quickly and take initiative is helpful but not required Ability to work independently in customer settings with minimal supervision Experience working with and managing hospital beds preferred IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  Note: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for 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 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 35-40 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 Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA.  IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. This part time position will be responsible for providing case support, patient management, and education to both new and existing accounts within an assigned client Franchise/Region.  Duties and Responsibilities: Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.Improve patient outcomes by delivering ventricular medical device education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.Ventricular medical device case support, including on call support.Complete proactive rounds for patients receiving support and provide assistance.Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessaryMaintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and educationSome travel may be neededJob Qualifications: Clinical certification required; Registered Nurse (RN)/Advanced Practice Provider (APP) license strongly preferred or relevant experience.3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred.Some industry experience preferred, but not required.Significant experience with ventricular medical device is required (minimum of 10 cases/patients supported).Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of availability per month.Availability must include (1) weekend per month.Ability to work on weekends, nights, holidays as well as weekdays.Ability to work at other hospitals aside from base location. Ability to clear hospital vendor credentialing requirements.Position may/will require up to date immunizations.#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 $60.00 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.

Clinical Trial Psych Rater - Romanian SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA 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. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Romanian. #LI-DNP #LI-Remote #LI-HCPN 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.

Clinical Trial Psych Rater - Czech SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA 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. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Czech. #LI-DNP #LI-Remote #LI-HCPN 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.

Clinical Trial Psych Rater - Slovak SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA 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. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Slovak. #LI-DNP #LI-Remote #LI-HCPN 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 is 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.

Job Overview Provide project related assistance to assigned project teams. Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements. Meeting quality and timeline metrics. Essential Functions Complete appropriate role-specific training to perform job duties.Under supervision, provides study level administrative support to the clinical study management team (examples of such tasks include, but not limited to running system reports, preparing and distributing status reports, creating and maintaining study trackers, follow-up for outstanding issues, etc.).Assist in updating and maintaining systems within project timelines/plans and driving tracking compliance in various systems to enable credible data for analysis.Perform the activities as per the task list delegated by CMS leads.Assist CMs in the preparation of i-site pack for their respective sites and countries for assigned studies, by pulling associated reports.Perform centralized monitoring activities on assigned sites and evaluate their quality and integrity as per the protocol, SOPs respective regulation and guidelines.Prepare i-site pack for respective sites and countries for assigned studies.Interact with sites/CRA and follow-up of missing data, pending queries, SDV backlog, visit schedule, PD, etc.Establish and maintain effective project/site communication.Assist leads in maintenance of internal systems, databases, tracking tools and project plans.Manage the operational insight of the assigned sites/studies and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).Perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.). Review any other information as necessary to determine overall readiness of the patient information for next level review.Perform Study specific analytics based on applicable study specific plans.Perform assigned access management related administrative tasks to support team members with project execution, example of tasks includes but not limited to processing access requests, following up with relevant vendors, assigning catalog task to process associates, etc.Act as a backup for Centralized Monitors/Sr. Centralized Monitors.Provide support to the technical solution specialist (TSS) on formulations in Excel, automations of tool using macros codes and designing of the tool on the front end and back end.Facilitating early identification of site-level risk/issue(s) occurring during study conduct and responsible for identification of risk.Monitor site performance and make recommendations for timely corrective actions (eg Site Telephone Contact or Triggered Onsite Monitoring Visit)Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observedReview of the Study Central Monitoring PlanAdhere to the key activities outlined in the SOW as per customer requirements.Qualifications Graduate/Post Graduate in Life Sciences or related field.Requires minimum of 2 to 5 years of work experience with minimum of 1 year relevant experience.Equivalent combination of education, training and experience. Experience level may vary based on customer specific requirements.Good knowledge of applicable clinical research regulatory requirements i.e., International Conference on Harmonisation - Good Clinical Practice and relevant local laws, regulations and guidelines.Proficient in Clinical Systems (good knowledge on electronic data capture (EDC), interactive X response system (IXRS), clinical trial management system (CTMS) or equivalent systems).Experience of managing global phase trials and clinical trial systems and/or reviewing clinical trial data.Strong written and verbal communication skills including good command of English language.Good command of Czech and Slovak language.Results and detail-oriented approach to work delivery and output.Good problem-solving skills.Good planning, time management and prioritization skills.Attention to detail and accuracy in work.Good software and computer skills, Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Strong telecommunication skills.Good data entry 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. The potential base pay range for this role, when annualized, is €18,400.00 - €27,600.00. 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.

We are seeking an experienced AI Solutions Architect to lead the design and delivery of next-generation AI solutions for pharmaceutical and life sciences organizations. This individual will help clients transform scientific, clinical, and operational data into explainable, trustworthy, and scalable AI solutions that accelerate research and development, improve decision-making, and drive innovation across the drug development lifecycle.     Role Overview As an AI Solutions Architect, you will combine your expertise in foundation models, knowledge graphs, agentic AI, and data architecture with strong consulting and client leadership skills. You will work closely with scientific, business, and technical stakeholders to design and deliver solutions that leverage next-generation AI capabilities and deliver measurable business value.     Key Responsibilities AI Solution Architecture  Lead the design and delivery of AI solutions across pharmaceutical research and development, translating business and scientific challenges into scalable solutions with measurable outcomes  Recommend appropriate architectures that align business objectives, data assets, and technology capabilities  Foundation Models and Agentic AI  Design and implement solutions using foundation models, large language models (LLMs), retrieval-augmented generation (RAG), and agentic AI frameworks  Define approaches for model selection, orchestration, grounding, prompt design, evaluation, validation, and production deployment    Knowledge Graphs and Semantic Systems  Architect biomedical knowledge graphs, ontologies, and semantic data models that support scientific discovery, reasoning, and intelligent information retrieval  Integrate knowledge graphs with foundation models to improve contextual understanding, explainability, and AI performance    Data Strategy and Engineering  Lead data integration, harmonization, and governance efforts across scientific, clinical, and operational data sources  Establish data foundations that support scalable, trustworthy, and AI-ready solutions    Client Leadership and Consulting  Serve as a trusted advisor to business, scientific, and technical stakeholders, leading workshops and solution design sessions  Communicate complex technical concepts to both executive and technical audiences, guiding clients from strategy through implementation    Innovation and Capabilities Development  Stay current on advances in AI, foundation models, and knowledge graphs, bringing emerging capabilities into solutions  Contribute to reusable methodologies, accelerators, and leading practices that scale AI delivery across engagements    What We're Looking For Master's degree or PhD in Computer Science, Bioinformatics, Computational Biology, Data Science, Engineering, or a related field.  Significant experience delivering AI, data, analytics, or digital transformation solutions in life sciences or pharmaceutical organizations  Demonstrated expertise in designing and deploying solutions leveraging foundation models, retrieval-augmented generation (RAG), agentic AI architectures, knowledge graphs, semantic technologies, vector databases, semantic search, machine learning, and predictive analytics  Experience designing AI solution architectures supported by strong data architecture principles.  Strong programming and solution development experience, particularly in Python and modern AI frameworks.  Experience with cloud platforms such as Azure, AWS, or Google Cloud.  Experience designing and deploying AI solutions in regulated environments.  Ability to translate complex business and scientific questions into structured AI solution designs and implementation plans.  Understanding of pharmaceutical R&D processes, including drug discovery, translational science, clinical development, safety, and regulatory approval.  Excellent communication, presentation, and consulting skills.  Ability to engage effectively with both executive stakeholders and highly technical teams.    Preferred Experience Experience designing and implementing biomedical knowledge graph solutions, including the integration of knowledge graphs with foundation models and agentic AI to support intelligent applications and scientific discovery.  Familiarity with biomedical ontologies, standards, and scientific data management practices, including FAIR data principles and semantic interoperability.  Experience establishing AI evaluation, validation, and governance frameworks, including benchmarking, human-in-the-loop review, and other quality assessment methodologies.  Understanding of the end-to-end pharmaceutical value chain, including R&D, regulatory affairs, market access, medical affairs, commercial operations, and post-marketing functions.  Experience leading client engagements and mentoring multidisciplinary technical teams.  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, when annualized, is $125,800.00 - $350,300.00. 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.

Consulting and Analytics in Germany is part of IQVIA’s Commercial and Consulting Services team in EMEA. The team supports healthcare and life science clients to make decisions across their commercial value chain, with the goal to create value for their brands and to improve patient care. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. You’ll have the opportunity to address challenging client issues, across multiple business areas with a hands-on influence in delivering solutions.  We operate in a truly multi-cultural and collaborative work environment that is rich in development and growth.  Are you interested in strengthening our team with your consulting expertise and to take on an opportunity where you can add significant value to the business of our Pharma and Life Sciences clients in an international environment? Your Responsibilities: As a Principal within Analytics & Consulting, you will take on a variety of roles that focus primarily within the following core areas: client/project leadership, business development, firm/operational leadership roles and supporting the recruitment committee with the selection of new staff as required. The main focus of a Principal is to deliver outstanding client service, while building trusted relationships with new and existing clients. In this role, you will: Act as principal owner of client engagements; owning responsibility for client satisfaction and delivering high levels of quality/added value strategies that address complex client issues. Develop close client relationships up to C-suite level at dedicated affiliate and / or HQ accounts in Germany. Create and elevate new business opportunities through the identification of value-added follow-on work and identify new revenue opportunities with existing and new client organizations. Allocate direction, advice, and intellectual leadership to clients and delivery teams. Form pursuit teams for larger engagements with the appropriate experts from the broader IQVIA organization during pre-sales, sales and delivery phases. Oversee the delivery in a Principal-in-Charge (PIC) role for projects in your area of expertise, with full responsibility vis-à-vis our clients for quality, time and budget.  Lead thought leadership and firm building initiatives. Remain current on industry, clients, and competitive trends and directions in order to anticipate and identify new business challenges and issues with assigned clients. Contribute to the enhanced awareness of Analytics & Consulting services in the marketplace, e.g. through speaking engagements, client meetings, and publications. Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients. Your Profile: Required Education and Professional Experience: A minimum of a Master’s degree or equivalent in business administration, business informatics/ engineering, health economics, natural sciences, medicine or related discipline, or knowledge acquired through equivalent experience. Extensive experience at a top consulting company, either general strategy; specialized or boutique consultancy. Sound, hands-on expertise in client delivery, project management and business development, incl. selling complex strategy and operations engagements to top Pharma/Life Sciences companies. Several years of project experience with pharma and other healthcare industries - sound knowledge of the pharma industry and its core processes is a must. Prior direct pharma industry experience is welcome. Additional Requirements: Entrepreneurial attitude and innovative mindset with a willingness to take risks and strong hunting skills, balanced with long-term strategic thinking for account development. Hands-on approach with strong issue-based consulting and conceptual skills, coupled with an ambition for innovation. Excellent listening and communication skills. Ability to lead and work collaboratively across complex networks, both internally and with clients, and to influence organizations. Proven ability to build relationships, identify client pain points, and develop custom solutions at the C-suite level. Excellent listening and communication skills. Proficiency in English is a must; fluency in German is preferred. Willingness to work in our Frankfurt/Munich/Berlin offices when not on-site with clients. Additional Skills and Experience:  Client Relationship Management and Delivery - Principal owner of client engagements to the commercial functions within leading Life Sciences organizations, focused on client satisfaction and outstanding client deliverables. Proven capability to identify new revenue opportunities with existing clients. Commercial Strategy and Analytics Experience - Ability to speak in detail with Senior Client Management about brand and commercial topics in the life sciences industry segment, in a meaningful manner with depth of content knowledge. Senior Level Solution Selling - Proven ability to build relationships, identify client pain points, and develop custom solutions with key clients stakeholders. Industry Trends - Maintains a constant focus on industry, client and competitive trends in the life sciences industry. Applies this knowledge to both active client engagements and business/client development activities. Team Development/Management - Proven skills in identifying, recruiting, mentoring/coaching, and retaining top talent for consulting practice teams.   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.

About the RoleIQVIA is looking for a Reference File Maintainer to support the acquisition, processing, and preparation of data received from suppliers. The role focuses on receiving, identifying, logging, and moving data through IQVIA acquisition platforms in line with standard operating procedures. The successful candidate will work under close guidance or supervision to ensure data is formatted appropriately for input into IQVIA systems. Key ResponsibilitiesReceive, identify, and log inbound data from suppliers.Replenish blank media to data suppliers as required.Execute the movement of data through IQVIA acquisition platforms according to standard operating procedures.Perform initial volume checks to determine whether the amount of data received is realistic.Required QualificationsHigh School Diploma or equivalent.Typically requires a minimum of 2 years of experience.At least 1 year of work experience.Basic job knowledge of systems and procedures gained through prior work experience or education.Skills and AbilitiesKnowledge of PC-based Windows applications, mainframe tools used by IQVIA, and third-party tools/software.Good interpersonal and communication skills.Ability to work effectively in a team environment.Ability to follow directions accurately and work under time constraints and changing work volumes.Ability to follow established procedures to resolve routine matters.Understanding of workflow and processes for different audits.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.

Clinical Trial Psych Rater - Serbian SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA 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. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S, SCID). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Serbian. #LI-DNP #LI-Remote #LI-HCPN 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 OverviewProvide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and close-out).  Ensure work is conducted in line with standard operating procedures, policies and good practices. Essential Functions• Study Setup and Planning:  Support the Project Manager by attending meetings, preparing minutes and action logs, preparing protocol-specific laboratory instructions documents. Under supervision of the Project Manager oversee setup of protocol specific Laboratory Centralized Monitoring requirements• Study Activity Monitoring and Closeout: Perform routine tasks across assigned studies including site loading, Investigator Portal access, kit shipments, monitoring day-to-day study performance, overseeing Laboratory Centralized Monitoring. Work with internal and external teams to manage timely resolution of queries and protocol questions, issues and escalations• Use status reports, monitoring tools and outputs to pro-actively identify trends and provide feedback to internal and external teams on performance of Investigator sites and company services. Support the Project Manager with administrative study tasks• Coordinate and communicate with relevant stakeholders, including leading Customer communications and activities during any times when the Project Manager is absent. Oversee Project Close-out• Meetings, Initiatives and Training Activities: May represent company at internal and external meetings, participate in external and internal audits/inspections. As required will support study training with sites, CRAs and customers• Ensure outputs are delivered in line with organizational standards, protocol specific requirements and Customer expectations Qualifications• High School Diploma or equivalent  Req Or• Bachelor's Degree Life sciences or related field Pref• 1+ years relevant experience (Clinical, Medical or Healthcare industry preferred).  Pref Or• Equivalent combination of education, training and experience.• Strong interpersonal, communication, organizational, and time management skills.• Must be able to comply with all applicable standards as required by the company.• Demonstrated ability to handle multiple competing priorities and utilize resources effectively.• Demonstrated ability of critical thinking and problem solving.• Strong written and verbal communication skills including good command of English language. In certain geographies where communication in local language is desired (e.g. Japan, China), excellent command of local language with reasonable proficiency in English preferred.• Computer proficiency in word processing, presentation and spreadsheet applications.• Demonstrated ability to work in a fast-paced environment highly desirable.• Ability to establish and maintain effective working relationships with coworkers and managers. 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.

Create and maintain PO Estimator (POE) calculation.• Manage PO creation, maintenance and closure.• Create, maintain, and close-out site-specific purchase requisitions in the local systems, utilizing the study-specific PO calculator, CTAs and CTMS for applicablecountries.• Run timely subject visit completion reports and enter data into CTMS.• Generate payments through CTMS, where applicable, and enter invoices into CTMS upon receipt to process ad-hoc payments.• Create and send payment notifications and/or reminders to sites and study teams to ensure timely payment.• Complete any RFI (request for invoice) and mismatches in a timely manner to avoid any business disruption.• Answer queries, questions and issue resolution with sites and study teams in a timelymanner.• Rectify failed payments, as appropriate, for purchase requisitions 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 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.

Clinical Specialist / Stroke Rater – Chinese Speaking Location: RemoteHours: Estimated 2–12 hours per month, flexible Role Overview The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rating patients using validated stroke scales and reviewing assessments performed by other raters to maintain protocol compliance and inter-rater reliability. Key Responsibilities Administer stroke-specific scales to trial participants (EQ-5D-5L (Interviewer administered and Proxy 1 version) & mRS).Review and evaluate assessments conducted by other raters for accuracy and adherence to protocol.Conduct live interactions with raters to provide feedback on scoring techniques and methodology.Participate in training, orientation, and calibration sessions to maintain certification and consistency.Prepare for rater discussions by reviewing case data and relevant documentation.Complete scheduled rater interactions and submit all required documentation promptly.Assist with mock interviews and functional assessments of rater performance as needed.Required Qualifications Education:Minimum: Master’s degree (MA/MS) in Medicine, Neurology, Psychology, or related field.Preferred: MD, DO, or PhD.Experience:At least 1 year of clinical experience with stroke patients.Prior experience administering stroke-related rating scales in clinical trials.Skills:Proficiency in EQ-5D-5L and mRS administration.Strong interpersonal and communication skills for professional interaction with raters and trial staff.Excellent organizational skills, attention to detail, and time management.Fluent Chinese language skills#LI-DNP #LI-Remote #LI-HCPN 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 OverviewApply knowledge and expertise including complex decision making activities to review, assess and process Safety data and information across service lines. Recognized as specialist in one or more areas. Provide oversight on small to medium service operational projects and act as mentor to junior members of staff. Key Responsibilities Process and manage safety cases, including adverse event intake, data entry, coding, narrative writing, quality review, and case follow-up activities. Assess case reportability and support regulatory submissions within required timelines. Perform pharmacovigilance activities in accordance with SOPs, regulatory requirements, and project-specific guidelines. Support activities across Safety services, including Safety Surveillance, Risk Management, Safety Publishing, and Medical Information where applicable. Maintain high standards of quality, compliance, productivity, and delivery. Provide training, mentoring, and day-to-day support to less experienced team members. Monitor project progress, metrics, and operational performance, escalating issues when needed. Collaborate with project management, clinical, data management, investigators, and clients to resolve project-related issues. Contribute to process improvements, training initiatives, and departmental goals. Participate in audits, inspections, and continuous improvement activities as required. Depending on project requirements, perform medical review of non-serious adverse events and ensure data quality, completeness, and regulatory compliance. Qualifications Bachelor's degree in Life Sciences, Pharmacy, Nursing, Healthcare, or a related scientific discipline. Up to 5 years of relevant experience, including up to 3 years of Pharmacovigilance experience. Strong understanding of pharmacovigilance processes, case management, and safety regulations. Excellent knowledge of medical terminology and safety databases. Strong organizational, time-management, and problem-solving skills. Excellent written and verbal communication skills. Ability to manage multiple priorities while maintaining high levels of accuracy and quality. Proven ability to work independently and collaboratively in a fast-paced environment. Strong mentoring, stakeholder management, and relationship-building skills. Proficiency with Microsoft Office and web-based applications. Experience with global pharmacovigilance regulations and industry standards. Experience supporting audits, inspections, and process improvement initiatives. Project coordination or leadership experience within a safety operations environment. Flexibility to work across global teams, different time zones, and shift schedules as required. 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.

Databricks & Snowflake Developer – Job DescriptionJob Summary: We are seeking an experienced Databricks & Snowflake Developer with strong expertise in PySpark, Delta Lake, Snowflake SQL, and Azure Data Engineering services. The ideal candidate will design, develop, and optimize large-scale data pipelines across both Databricks and Snowflake platforms to support analytics, reporting, and enterprise data initiatives.This role requires close collaboration with data engineers, analysts, architects, and business stakeholders to deliver scalable, high‑quality, and cost‑efficient cloud data solutions.  Key Responsibilities 1. Databricks Development Develop, optimize, and maintain Databricks Notebooks, Workflows, and Jobs.Build scalable PySpark applications and data transformations.Implement and manage Delta Lake tables, including schema evolution and performance tuning.Use Git-based version control for notebook and code management. 2. Snowflake Development Develop and optimize Snowflake SQL, including complex joins, window functions, and CTEs.Build and manage Snowflake pipelines using Stages, File Formats, COPY, and Snow pipe.Implement Streams, Tasks, Materialized Views for automated ELT workflows.Manage Snowflake performance tuning, virtual warehouse optimization, and cost governance.3. Data Pipeline & ETL/ELT Engineering Design and build data pipelines integrating Databricks, Snowflake, and Azure Data Factory.Implement ETL/ELT flows using Spark, SQL, Snowflake pipelines, and ADF/Synapse.Optimize pipelines for scalability, performance, and cost efficiency. 4. Data Integration Integrate data from relational databases, APIs, file systems, and cloud platforms into Databricks and Snowflake.Ensure alignment with enterprise data architecture and modeling standards. 5. Documentation & Compliance Document all pipelines, workflows, data models, and architecture across Databricks and Snowflake.Ensure compliance with governance, security, and regulatory standards. 6. Collaboration Work with business stakeholders to gather data requirements and convert them into technical solutions.Support BI, analytics, and downstream consumers across both platforms. 7. Troubleshooting & Support Debug Databricks issues including notebook failures, Spark job errors, and ADF pipeline failures.Troubleshoot Snowflake execution errors, warehouse performance problems, and ingestion failures.Perform root‑cause analysis and implement preventive measures. Qualifications Education Bachelor's degree in Computer Science, Information Technology, or related field (or equivalent experience). Experience 4+ years of experience in data engineering or big data development.3+ years hands‑on with Databricks, PySpark, and Azure Data Engineering.3+ years hands‑on with Snowflake, Snowflake SQL, and ELT development.(Databricks components)Technical Skills Databricks Strong hands-on experience with Databricks, PySpark, Delta Lake, Spark SQL.Experience with ADF, Synapse, and ADLS integrations. Snowflake Expert in Snowflake SQL, performance tuning, and warehousing.Experience with Snowpipe, Streams, Tasks, and orchestration via ADF/Synapse.Knowledge of RBAC, masking policies, and security best practices.General Strong understanding of data warehousing concepts and cloud data architecture.Familiarity with CI/CD (Azure DevOps/GitHub Actions) and Git workflows. Soft Skills Strong analytical and problem‑solving abilities.Excellent communication and stakeholder management.Ability to work independently and collaboratively in agile teams. Company Culture Our company values innovation, teamwork, and continuous learning. We encourage creativity and provide opportunities for professional growth. 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.

Join global organization with 82000+ employees around the world, as a Decipher Programmer based in IQVIA Bangalore .You will be part of IQVIA’s world class technology team and will be involved in design, development, enhanced software programs or cloud applications or proprietary products. Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions. Essential Functions Develop online survey using effective survey programming tools, viz. Decipher.Assist in medium to complex custom scripts using jQuery/ JavaScriptProactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.Engagement based responsibilities are assigned and managed by Consultants, Senior Consultants, Engagement Managers or Principals.Strong analytical and problem-solving skillsAbility to work in a fast-paced environment and manage multiple projects simultaneously Qualifications A bachelor’s or master’s degree2-5 years of related experience requiredWorks willingly and effectively with others in and across the organization to accomplish team goals.Knowledge of data processing/ analysis tools, viz. SPSS, Wincross is a good to have skill.Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.Knowledge of consulting methods, tools, and techniques, related to one’s functional area.Knowledge of current events and developments within an industry and major competitors.Effective time management 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.

Medical Sales Representative – Adelaide NorthContract Opportunity | IQVIA Partnered with a Global Pharmaceutical LeaderIQVIA is partnering with one of our leading pharmaceutical clients to recruit a Medical Sales Representative in Adelaide North. In this role, you will work alongside the client's established sales team, building strong relationships with healthcare professionals and helping drive positive patient outcomes through innovative healthcare solutions. About the Role As a Medical Sales Representative, you’ll be the face of innovative prescription products, building strong relationships with General Practitioners and Pharmacists across your territory. Your mission: Educate and engage healthcare professionals on our product portfolio. Drive sales growth and achieve targets through strategic territory management. Collaborate with cross-functional teams to deliver exceptional results. This is an exciting opportunity to combine your commercial acumen with a genuine passion for healthcare. What We’re Looking For Degree qualified in Life Sciences, Business, or related field. Proven success in medical sales or similar B2B environment. Strong communication, presentation, and negotiation skills. Ability to thrive in a target-driven, dynamic setting. Commitment to ethical standards and patient care. Why Join Us? Work with a global leader in pharmaceuticals. Access to industry-leading training and resources. Be part of a supportive, high-performing team that values growth and innovation. Ready to make a difference?Apply now and take the next step in your career while helping transform patient care. 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.