IQVIA

Essential Functions Works with customers and project management teams to identify key project milestones and implementation timelines.Builds, documents and maintains new and existing customer-centric business critical solutions.Develops and implements solution validation plans.Ensures quality control during implementation and execution of the validation plans.Builds training materials for the implemented solutions.Trains customers on the implemented solutions.Participates in QA, UAT & production launch support related to various customer engagements.Contributes towards building implementation and integrations best practices and the knowledge base.Collaborates with the DrugDev product development team to help improve and expand core platform functionality.Provides Tier 2/3 technical support for custom integrations.Has working knowledge of support processes and working in production environment.Works with customers and project management teams to identify key project milestones and implementation timelines.Qualifications Bachelor's Degree Computer Science, a related field, or equivalent experienceExperience working with external customers to gather technical requirementsPrefWorking knowledge of software development processes and methodologies ReqKnowledge of the clinical trial / pharmaceutical domain PrefPowerful work ethic with a focus on customer satisfaction IntermediateStrong customer facing and presentation skills IntermediateProcess documentation skills IntermediateValidation documentation and execution skillsIntermediateTechnical troubleshooting and documentation skills IntermediateIQVIA 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.

External Job DescriptionTo be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred.• Requires at least 3 years of year of on-site monitoring experience.• Equivalent combination of education, training and experience may be accepted in lieu of degree.• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $74,500.00 - $197,500.00. 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.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 50 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Collaborate with  pre and post award stakeholders to manage the coordination, planning, and implementation of Patient Recruitment and Retention support operational plans on larger, multi- region studies or programs. Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan; make proactive operational and tactical recommendations as needed based on study performance.  Collaborate with internal teams and external providers to deliver all appropriate tactics associated with the recruitment/retention strategy. Represent IQVIAs Patient Recruitment at site/sponsor-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required. Ownership for study KPI and financial performance. Act as senior oversight for large studies / programs leading a team and taking overall ownership for study performance. Essential Functions• Work together with the strategy team to translate recruitment and retention strategy into operational and tactical plans to positively impact recruitment and retention rates for assigned projects• Serve as internal consultant to project teams to implement operational recruitment plans on new and/or existing projects needing recruitment and retention services• Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects (based on scope, may co-manage or independently manage these projects)• Serve as primary operational project contact for patient recruitment and retention programs with sponsor (or as escalation point where acting as oversight) to ensure appropriate communication channels are maintained and reporting schedules adhered to as required• Management of assigned project budget(s) to meet financial and company goals (realization targets)• Coordinate operational and tactical related project activities for study team and sponsor to ensure that overall project milestones are met• Develop and implement risk management plans for minimizing impact on project objectives and deliverables• Other duties as assigned by Management• Maintain knowledge of current recruitment trends, vendors, and technologies to increase productivity and recommend additional support as needed• Leverage internal intelligence to support and refine strategy on assigned projects• Provide technical expertise as able in support of project specific and interdepartmental training efforts• Support continued process improvement to ensure quality in the department. Qualifications• Around 6 years of relevant industry experience in a role with global exposure (not local), ideally in a patient recruitment role (please, be aware this is NOT a talent acquisition specialist/recruiter role)• Good project management skills: to be able to create budget and review it along with the sponsor plus manage different proposals at the same time.• Good presentation skills / client facing skills.• Good written and verbal communication skills including good command of English - you will be working in a global team.• Ability to influence effectively within SPN/PRP team and project teams including TSL, PL, CL, CRA and the customer. #LI-NRJ #LI-Remote 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.

We are seeking a highly motivated pharmacovigilance professional to join our Safety Aggregate Report & Analytics (SARA) team. This is an exciting opportunity to take a leading role in safety reporting, signal management, and benefit-risk evaluation activities supporting both marketed and investigational products worldwide. Working in a highly collaborative and international environment, you will partner with cross-functional stakeholders, advise clients, and contribute directly to the safety strategies that help protect patients across the globe. What You'll Do Lead the preparation and delivery of key aggregate safety reports, including PBRERs/PSURs, DSURs, PADERs, RMPs, ACOs, and line listings. Serve as the primary owner of assigned safety deliverables, ensuring quality, compliance, and on-time execution. Lead signal management activities, including: Signal detection, validation, and evaluation Risk assessment and characterization Documentation and tracking of safety signals Development and execution of signaling strategies Conduct and oversee literature surveillance for commercialized and investigational products. Author responses to regulatory authority inquiries and support safety labeling and benefit-risk documentation. Collaborate with global stakeholders across Pharmacovigilance, Regulatory Affairs, Medical Writing, Clinical Research, Quality, Safety Operations, and other functional teams. Provide mentorship and guidance to junior team members. Support audits, inspections, process improvements, and innovation initiatives. Drive project success through effective stakeholder management, communication, and leadership. What We're Looking For Bachelor's degree in Life Sciences field. 2-4 years of post-marketing pharmacovigilance experience covering aggregate reporting, signal management and benefit-risk assessment. Excellent level of English. Strong understanding of global pharmacovigilance regulations and guidelines, including GVP, GCP, and ICH. Experience authoring or leading aggregate safety reports and regulatory deliverables. Strong project management and stakeholder management skills. Excellent analytical thinking, attention to detail, and written communication abilities. Ability to work independently while managing multiple priorities in a fast-paced global environment. Grade: 140 Work modality: home based. Why Join Us? - Work on high-impact global safety programs that contribute directly to patient safety. - Collaborate with international teams and leading pharmaceutical and biotech clients. - Expand your expertise across aggregate reporting, signal management, risk management, and regulatory strategy. - Grow your leadership skills through mentorship, client interaction, and project ownership. - Be part of a team that values innovation, continuous learning, and professional development. If you're passionate about pharmacovigilance and ready to take ownership of complex safety activities in a global environment, we'd love to hear from you. 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 OverviewReview, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This role requires fluency in English and Spanish. Main Responsibilities Process safety data according to applicable regulations, guidelines, SOPs, and project requirements. Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities. Ensure compliance with quality, productivity, and delivery standards per project requirements. Liaise with different functional team members and healthcare professionals to address project-related issues.  Qualifications Bachelor’s degree in Life sciences or a related field (mandatory) Fluency in English and Spanish (mandatory) Up to 3 years of previous clinical experience (desirable) 1 year of pharmacovigilance experience will be highly valued (desirable) Work modality: 100% home-based What we offer to you: OSDE 310 Annual bonus by performance Salary adjustments during the year according to inflation rates. 21 vacations days Work flexibility 100% remote role! 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 RPM will provide business support to GRA. Key member of the Project Management Team ensuring the Product strategy aligns with the Regulatory strategy and works in concert with the PMT and GRT to operationalize the plans.  Provides cross-functional leadership to the submission teams in developing and executing the submission plans for Global filings. Creates and owns the regulatory project plans and develops project and portfolio level reports utilizing various systems to support key decision making. Deliverables: Will provide project management support for the regulatory end-to-end process from entry into late development through launch. Will represent “Regulatory Program Management” at the GRT. Translate regulatory strategy into realistic and executable regulatory deliverables with clear assumptions based on GRT input through leveraging of the Regulatory Strategy Document and Risk Registry Works out regulatory scenarios to support decision making in line with Regulatory and CDT strategy. Supports early risk identification and development of mitigation strategies. Works in close collaboration with the Regulatory Leader (GRL) to proactively prepare regulatory activities to be discussed in the GRT. Works in close collaboration with the Regulatory Liaisons and Professionals to work out NA-EMEA-APJLA specific details on Health Authority interactions and submissions. Support Global filings across all regions; Initiate discussion, establish the Global filing plan and verify submission groups; maintain appropriate plans in the team Sharepoint site; ensure execution of the plans through discussion at the global and regional levels, assessing requirements and risks, monitoring progress and assessing critical path, and planning for submission roll out based on priorities. Works in close collaboration with Submission Operations for timing of pre-submission activities. Is single Point of Contact for “Regulatory Program Management” activities. Proactively plans and manages the cross-functional project deliverables that support the global regulatory strategy and worldwide submissions (NA – EMEA - APJLA). Active follow-up on the progression of all regulatory activities required to successfully and timely complete the regulatory deliverables (Health Authorities interactions, submissions, etc.). Monitors regulatory driven key milestones, decision points and critical path activities. Creates project related reports to support decision making at PMT, GRT and CDT level, supports regulatory portfolio oversight, supports team member planning of short- and long-term deliverables. Informs stakeholders on project deliverables status. Assists GRT’s in determining resource requirements utilizing scheduling and resource management tools to support early and late development teams, depending on TA and R&D needs. Coordinates the creation, maintenance, management and timely submission of regulatory project budgets (OOPs & FTEs). Owns the Regulatory tasks in the Planisware platform V6 program schedule; responsible for the creation, monitoring and maintenance. Owns the Regulatory schedule in MSPS16; responsible for the creation, monitoring and maintenance of the timelines.  Depending on program plans this activity can start as early as Phase I Health Authority Interactions and extends through Initial Filings and into subsequent add-on submissions. Owns the Submission plan in MSP 16; creation, monitoring and maintenance. Creates visuals utilizing OnePager, OfficeTimeline, or Swimlane. Represents “Regulatory Program Management” at the PMT. Works in close collaboration with the CDT Program Management Leader (CDT-PML) to ensure alignment of the regulatory strategy with the CDT strategy. Works in close collaboration with the PMT Program Managers to ensure alignment of functional strategies with the regulatory strategy. Proactively manages the regulatory development plan (scope, time, cost). Is single Point of Contact for “Regulatory Program Management” Activities. Profile: B.S. or advanced degree in pharmaceutical-related subjects. Professional project management certification is a plus. Regulatory Affairs Certificate is a plus 5 years of relevant experience including at least 3-5 years in (bio)pharmaceutical R&D. Experience in big matrix organization is preferred. The key requirement is strong program-level experience, particularly in managing trials and studies at the compound level. Project management experience in R&D drug development is a must. Detailed knowledge of: project planning, tracking, resource management, project planning and scheduling tools, and cross-project analyses. Registration experience with global submissions pre and post marketing is preferred. Understanding of Regulatory processes, both pre- and post-marketing. Working knowledge of regulations, guidelines and regulatory requirements is preferred; such as health authority requirements and Global CoPP needs. The RPM will provide business support to GRA. Key member of the Project Management Team ensuring the Product strategy aligns with the Regulatory strategy and works in concert with the PMT and GRT to operationalize the plans.  Provides cross-functional leadership to the submission teams in developing and executing the submission plans for Global filings. Creates and owns the regulatory project plans and develops project and portfolio level reports utilizing various systems to support key decision making. Deliverables: Will provide project management support for the regulatory end-to-end process from entry into late development through launch. Will represent “Regulatory Program Management” at the GRT. Translate regulatory strategy into realistic and executable regulatory deliverables with clear assumptions based on GRT input through leveraging of the Regulatory Strategy Document and Risk Registry Works out regulatory scenarios to support decision making in line with Regulatory and CDT strategy. Supports early risk identification and development of mitigation strategies. Works in close collaboration with the Regulatory Leader (GRL) to proactively prepare regulatory activities to be discussed in the GRT. Works in close collaboration with the Regulatory Liaisons and Professionals to work out NA-EMEA-APJLA specific details on Health Authority interactions and submissions. Support Global filings across all regions; Initiate discussion, establish the Global filing plan and verify submission groups; maintain appropriate plans in the team Sharepoint site; ensure execution of the plans through discussion at the global and regional levels, assessing requirements and risks, monitoring progress and assessing critical path, and planning for submission roll out based on priorities. Works in close collaboration with Submission Operations for timing of pre-submission activities. Is single Point of Contact for “Regulatory Program Management” activities. Proactively plans and manages the cross-functional project deliverables that support the global regulatory strategy and worldwide submissions (NA – EMEA - APJLA). Active follow-up on the progression of all regulatory activities required to successfully and timely complete the regulatory deliverables (Health Authorities interactions, submissions, etc.). Monitors regulatory driven key milestones, decision points and critical path activities. Creates project related reports to support decision making at PMT, GRT and CDT level, supports regulatory portfolio oversight, supports team member planning of short- and long-term deliverables. Informs stakeholders on project deliverables status. Assists GRT’s in determining resource requirements utilizing scheduling and resource management tools to support early and late development teams, depending on TA and R&D needs. Coordinates the creation, maintenance, management and timely submission of regulatory project budgets (OOPs & FTEs). Owns the Regulatory tasks in the Planisware platform V6 program schedule; responsible for the creation, monitoring and maintenance. Owns the Regulatory schedule in MSPS16; responsible for the creation, monitoring and maintenance of the timelines.  Depending on program plans this activity can start as early as Phase I Health Authority Interactions and extends through Initial Filings and into subsequent add-on submissions. Owns the Submission plan in MSP 16; creation, monitoring and maintenance. Creates visuals utilizing OnePager, OfficeTimeline, or Swimlane. Represents “Regulatory Program Management” at the PMT. Works in close collaboration with the CDT Program Management Leader (CDT-PML) to ensure alignment of the regulatory strategy with the CDT strategy. Works in close collaboration with the PMT Program Managers to ensure alignment of functional strategies with the regulatory strategy. Proactively manages the regulatory development plan (scope, time, cost). Is single Point of Contact for “Regulatory Program Management” Activities. Profile: B.S. or advanced degree in pharmaceutical-related subjects. Professional project management certification is a plus. Regulatory Affairs Certificate is a plus 5 years of relevant experience including at least 3-5 years in (bio)pharmaceutical R&D. Experience in big matrix organization is preferred. The key requirement is strong program-level experience, particularly in managing trials and studies at the compound level. Project management experience in R&D drug development is a must. Detailed knowledge of: project planning, tracking, resource management, project planning and scheduling tools, and cross-project analyses. Registration experience with global submissions pre and post marketing is preferred. Understanding of Regulatory processes, both pre- and post-marketing. Working knowledge of regulations, guidelines and regulatory requirements is preferred; such as health authority requirements and Global CoPP needs. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Registered Dietitian – Clinical Research Support Location: Remote (Romania) Job Type: Freelance / Part-time (ad hoc hours) Are you ready to make a real impact? Do you want to work flexibly from anywhere in Romania, while advancing your career with a global leader in healthcare innovation? Join IQVIA and become part of a collaborative, forward-thinking team that values your expertise and supports your professional growth. IQVIA is seeking experienced and registered Dietitians to join our team for an international clinical research projects in the field of metabolic disease area. You will support patients participating in clinical studies, provide nutritional and lifestyle guidance, and contribute to improving healthcare outcomes. Key Responsibilities Conduct comprehensive nutritional assessments Provide ongoing counseling and motivational support to study participants Monitor participant progress and outcomes throughout the study period Conduct all meetings and consultations with participants online (telehealth) Collaborate with the clinical research team to ensure adherence to study protocols Maintain accurate and confidential documentation in compliance with regulatory standards Participate in virtual team meetings and training sessions Requirements Certified and Registered Dietitian Fluent in Romanian and English; additional language skills are a plus Strong interpersonal and communication skills Ability to work independently and in a structured manner; clinical experience preferred Proficient with digital tools and telehealth platforms What We Offer Opportunity to contribute to a high-impact international clinical study Remote work and collaboration with an international team All participant interactions and monitoring are conducted online Professional development and exposure to global research standards Why IQVIA? At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research. #LI-DNP #LI-CES #LI-HCPN #LI-XS 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.

We are recruiting a team of Medical Sales Representatives to join a dedicated field team working within digestive health in Romania.This is a territory‑based role focused on building strong, professional relationships with healthcare professionals across an assigned geographic area. You will represent a structured healthcare project, delivering high‑quality, compliant medical and commercial interactions with Gastroenterologists and Internal Medicine physicians, and engaging pharmacies where appropriate. Your roleTake full ownership of a defined geographic territory in Romania, planning and executing all field activityBuild long‑term professional relationships with specialist healthcare professionals within your territoryDeliver clear, compliant medical and commercial discussions following structured trainingExecute effective territory planning, balancing call frequency, coverage and call qualityAchieve agreed activity and performance objectives for your territoryUse CRM systems to plan, prioritise and document customer interactions accuratelyEngage pharmacy stakeholders where relevant as part of the local territory strategyOperate fully in line with Romanian regulations, industry codes and internal compliance standardsWhat we’re looking forQualified to work as a medical sales representative in RomaniaFluent in Romanian (spoken and written)Bachelor’s degree in Life Sciences or a related discipline, or equivalent experienceExperience in pharmaceutical, medical or healthcare salesStrong communication skills and the ability to build credibility with specialist HCPsWell‑organised, resilient and comfortable working independently across a territoryConfident using CRM systems and digital toolsValid driving licence and willingness to travel extensively within the assigned territoryWhy this roleA clearly defined territory with ownership and accountabilityWork within a broad, clinically relevant therapy area central to routine medical practiceStructured onboarding, training and ongoing support within a professionally managed projectAvailable Territories: Bucuresti | Transilvania & Banat | Moldova#LI‑CES #LI-DNI 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 recruiting a Brand Manager to act as the brand lead for one or more specialty care brands on behalf of one of our pharmaceutical partners. This role offers the opportunity to take ownership of brand strategy and execution for medicines promoted within specialist healthcare settings, operating in a multi‑country, matrix environment. The assigned brand(s) sit within a broader partner portfolio spanning immune‑mediated and inflammatory diseases, including a mix of injectable biologics and oral advanced therapies. The Brand Manager will be accountable for shaping brand direction, translating insights into action, and delivering effective, compliant marketing activity that supports agreed commercial objectives. Working closely with IQVIA cross‑functional teams and partner stakeholders, this role requires strong commercial judgement, collaboration and the ability to balance strategic planning with hands‑on execution in a regulated pharmaceutical environment. Key ResponsibilitiesAct as the brand lead for one or more assigned brands, with end‑to‑end accountability for strategy and execution Develop and deliver integrated brand plans aligned to partner objectives and portfolio priorities Translate market, customer and patient insights into clear positioning, messaging and campaigns Lead multi‑channel / omnichannel marketing initiatives across field, digital, congress and remote channels Ensure consistent, compliant brand storytelling across all customer touchpoints Work closely with Sales, Medical, Market Access, Regulatory, Legal/Compliance and Operations teams Collaborate with partner stakeholders to ensure alignment and high‑quality execution Support field teams with approved brand materials and messaging Manage agencies and vendors, including briefing and delivery of marketing assets Own brand‑level budgets, forecasts and spend tracking Monitor performance against KPIs, including campaign effectiveness and ROI Use data and insights to continuously optimise brand performance Conduct market research and competitive analysis Ensure all activities comply with IQVIA SOPs, partner requirements and industry codes ExperienceEssential Experience in pharmaceutical brand or product management, ideally within specialty or secondary care Demonstrated experience leading individual brands within a broader portfolio Strong strategic thinking combined with hands‑on execution capability Proven ability to work effectively in matrix and multi‑stakeholder environments Strong analytical and commercial mindset Excellent communication and stakeholder‑management skills Desirable Experience in dermatology Exposure to multi‑country or regional brand roles Experience working with biologic and/or oral therapies Omnichannel marketing experience within a regulated environment Apply NowIf you are a Brand Manager looking to take ownership of one or more specialty care brands within a high‑impact, partner‑led environment, we encourage you to apply. #LI-CES #LI-CS1 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.

Provide support and assistance to project managers and project teams related to the assigned project(s). Will support all project-related activities for assigned projects in accordance with SOPs, policies and practices. Essential Functions • Establish new processes and improve upon existing processes related to project support. • Lead the set up and maintenance of all project documentation files and records according to the scope of work and SOPs. • Create and coordinate all information and communications for assigned projects. • Develop training materials related to new project deliverables. • Update and maintain internal databases, tracking systems and project plans with project specific information. • Prepare, analyze and distribute status, tracking and costs of specific project deliverables. • Prepare presentation materials for meetings and project summary data. • Create and establish SOPs and procedures for specific tasks assigned to a project. • Coordinate project team and customer meetings, identifying and planning appropriate medium (Web, telecon, face to face) and ensuring arrangements are handled appropriately. Determine and plan all meeting requirements in advance. • Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly. • Create and track project timelines • Articulate with others project support staff within and across the organization to identify and consolidate support processes. • Will serve as primary backup contact for internal project team and for external stakeholders/customers as designated by project manager. • Will undertake project management activities as directed by project manager • Train and mentor more junior project support staff. Qualifications • Bachelor's Degree in Industrial Engineering or Administrative degrees • 6 months of related experience • Strong communication and interpersonal skills • Advanced level of MS Office applications • Intermediate English Level 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 OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with  applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions• Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site regulatory documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory and contractual documents for individual sites.• Distribute completed documents to sites and internal project team members.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Qualifications• Bachelor's Degree Life sciences or a related field (required).• 1 years of experience in a healthcare environment or clinical research. Experience as an Intern or Study Coordinator can be accepted. • Availability to go to office: Hybrid position.• Good interpersonal communication and organizational skills.• Good word processing skills and knowledge of MS Office applications.• Good attention to detail.• General awareness clinical trial environment and drug development process.• Ability to work on multiple projects.• Ability to establish and maintain effective working relationships with co-workers, managers and sponsors. 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.

¡Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Profesional / Enfermeea de Acceso PSP Actualmente nos encontramos en la búsqueda de profesionales del área de la salud que quieran ser parte de un gran proyecto con una importante farmacéutica multinacional para PSP. Objetivo del cargo El Profesional de Acceso / Enfermera Gestora Administrativa es responsable de facilitar, acelerar y asegurar la continuidad del proceso administrativo para que los pacientes del programa cuenten con acceso oportuno a los medicamentos, mediante la gestión experta dentro de EPS, IPS y operadores logísticos. Este rol no tiene contacto con pacientes. Su función es apoyar al equipo de educadoras, resolviendo barreras administrativas, gestionando autorizaciones, agilizando cortes y articulando directamente con actores clave dentro del sistema de salud colombiano. Principales Funciones: Gestión y Aceleración del Acceso Gestionar, revisar y acelerar procesos administrativos relacionados con: Autorizaciones, renovaciones, radicaciones, validación de requisitos, conciliación de información en EPS y operadores. Identificar barreras administrativas en tiempo real y resolverlas mediante relacionamiento estratégico. Revisión y Movilidad de Cortes Monitorear los cortes administrativos de pacientes del programa. Validar tiempos de entrega, consumos y estados administrativos con operadores logísticos. Prevenir interrupciones en la continuidad del tratamiento mediante intervención temprana. Escalar inconsistencias a niveles superiores dentro de EPS/IPS cuando sea necesario. Relacionamiento con EPS, IPS y Operadores Logísticos Mantener relación directa, formal y estratégica con áreas clave: Autorizaciones, auditoría médica, compras, farmacia, direcciones médicas y administrativas. Gestionar reuniones, visitas y espacios de articulación para fluidificar procesos. Ser el punto de contacto técnico-administrativo entre el PSP y las entidades del sistema. Soporte al Equipo de Navegadoras/Educadoras Brindar acompañamiento administrativo especializado para: resolver escalaciones institucionales, desbloquear solicitudes complejas, alinear procesos con áreas internas y externas. Generar rutas eficientes de gestión para que las navegadoras puedan concentrarse en el soporte al paciente. Reportes y Documentación Registrar todas las gestiones en plataformas definidas por el PSP. Preparar reportes, indicadores y análisis de: Tiempos de autorización, tiempos de dispensación, causales de barreras, eficiencia institucional. Cumplir lineamientos de calidad, privacidad y compliance. Requisitos Carrera Profesional en Enfermería (deseable) o profesional en áreas de la salud con alto conocimiento del SGSSS. Tarjeta profesional vigente Deseable formación en auditoría, aseguramiento, gestión del riesgo o administración en salud. Mínimo 3 años comprobados de experiencia en: EPS, IPS u operadores, en áreas de autorizaciones, compras, auditoría o farmacia Experiencia en acceso de ruta oncológica (indispensable) Conocimiento de los procesos internos del SGSSS, incluidos MIPRES, rutas integrales y modelos de contratación. Relacionamiento comprobado con EPS de alto volumen en Colombia. Dominio profundo del sistema de salud colombiano. Experiencia sólida en: procesos administrativos, financieros y asistenciales dentro de EPS/IPS, operación de plataformas administrativas y de validación e identificación y resolución de barreras de acceso. Manejo avanzado de Excel y plataformas de registro. Habilidad para negociar y comunicarse con múltiples stakeholders. Alta capacidad de análisis y resolución. Organización y manejo de múltiples procesos simultáneos. Orientación a resultados y eficiencia operativa. Disponibilidad para viajar y trabajar 100% en campo. Residencia: Bogotá #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

JOB OVERVIEW Provide support and guidance to less experienced members of an HR team in their day-to-day operational roles.  Support the continuous improvement of the HR function, through development and implementation for all HR programs in an assigned geography or assigned business line.  With limited guidance, provide HR support to employees and management across assigned service areas, business units, or departments. As HR Business Partner, with guidance, provide expertise, support and advice to assigned management teams either locally, regionally, globally or by function.  Responsibilities Develop strong and effective team relationships with HR specialist functions/Centers of Excellence, e.g., HRPSC, Finance PSC.Support line managers in the process of new employee orientation where appropriate.Conduct ad hoc reviews as directed and propose recommendations in handling employment legislation, compliance, HR systems, practices and procedures and, with guidance, provide support and education to line management.Participate as assigned, with minimal supervision, in working with senior HR team members in the day-to-day development and implementation of new local and global HR initiatives.Work with more experienced HR team members on organizational effectiveness and HR partnering change management efforts associated with reorganizations, mergers/acquisitions and transfers to ensure compliance to local legislation.Provide reports and analyses as requested by senior management.Support line managers in the recruitment and selection process where appropriate.Operate as first point of contact for HR-related queries and work in conjunction with senior members of the HR team and line management on issues.Requirements Bachelor's and above degree3 years above experience within an HR function as a generalist or combination of generalist and specialist experienceExtensive knowledge of local and relevant employment legislationStrong computer skills, including Microsoft Office applications and HRIS applicationsExcellent problem solving, judgment and decision making skillsStrong verbal and written communication skillsGood presentation skillsGood influencing skillsGood coaching and counseling skillsVery high degree of discretion and confidentialityStrong attention to detailAbility to multi-task, prioritize and plan routine activitiesGood ability to work in a matrix environmentAbility to establish and maintain effective working relationships with coworkers, managers and clientsIQVIA 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.

Product Manager – Data ProductsRole Overview We are seeking a strategic and customer-focused Product Manager to lead the vision, roadmap, and delivery of data products that drive business value and innovation. This role will partner closely with engineering, analytics, and business stakeholders to develop scalable data solutions, prioritize investments, and ensure successful product outcomes. The ideal candidate combines strong product management expertise with a solid understanding of modern data platforms and infrastructure. Key ResponsibilitiesBuild and execute a product roadmap that delivers incremental value and drives the achievement of clearly defined business objectives.Develop strong cross-functional relationships, earning the trust and respect of stakeholders, engineering teams, and business partners.Contribute to product strategy and make informed trade-off decisions based on business priorities, market dynamics, customer needs, and technical considerations.Understand market, industry, and customer requirements and translate them into product features, capabilities, and use cases.Apply best-practice product management methodologies to drive a product-led approach to prioritization, solution design, and execution.Lead product discovery efforts to improve predictability, maximize ROI, and ensure investments are aligned with business outcomes.Partner with engineering and data teams to ensure products are scalable, reliable, secure, and well-supported.Support product launches, stakeholder communications, product marketing, and sales enablement through effective coordination, documentation, and presentations.Drive adoption and continuous improvement by gathering user feedback, monitoring performance metrics, and identifying opportunities for enhancement.Desired Experience & SkillsStrong product management experience with a track record of delivering impactful digital or data-driven products.Data product leadership experience strongly preferred, including ownership of data platforms, analytics products, reporting solutions, or data services.Understanding of data modeling, data pipelines, Snowflake infrastructure, and API design is highly desirable.Familiarity with Atlassian Confluence and Jira for product planning, documentation, and agile delivery.Experience working in Agile/Scrum environments and collaborating with technical and non-technical stakeholders.Strong analytical, problem-solving, and communication skills.Ability to translate complex technical concepts into clear business value propositions.QualificationsBachelor's Degree in Computer Science, Information Systems, Engineering, Business, or a related field, or equivalent practical experience.Experience managing technical, data, or platform products in a fast-paced environment.Demonstrated ability to balance customer needs, business goals, and technical feasibility while delivering measurable outcomes.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.

Senior Product Manager, ProviderJoin a team building data-driven products that sit at the heart of how hospitals and health systems grow and operate. As a Senior Product Manager on the Provider Solutions portfolio, you’ll turn complex healthcare data into actionable insights, helping organizations analyze referral patterns, close care gaps, forecast demand, and empower physician engagement strategies. This is a highly hands-on role for someone who thrives in an engineering-driven environment, can quickly translate business problems into scalable product solutions, and is eager to deliver measurable impact for provider organizations navigating an increasingly competitive healthcare landscape.Job Description SummaryOwn day-to-day product management for Provider Solutions offerings by translating product strategy into clear execution. Define and drive an actionable roadmap aligned with customer value, business priorities, and measurable outcomes. Partner cross-functionally with engineering, data/analytics, design, and commercial leadership to deliver capabilities that enable healthcare organizations to improve decision-making and performance. Job OverviewThe Senior Product Manager, Provider is responsible for driving execution across multiple Provider Solutions products. This role ensures alignment between product delivery, customer needs, and business objectives by developing clear product requirements, managing prioritization, and delivering measurable value. The role requires strong collaboration across cross-functional teams and a focus on continuous improvement through data and market insights. Essential FunctionsOwn day-to-day product execution across multiple Provider Solutions offerings, ensuring alignment with customer value and portfolio prioritiesTranslate product strategy into an actionable roadmap by defining themes, prioritizing initiatives, and maintaining a well-curated backlogAlign product delivery with business objectives by balancing customer needs, commercial priorities, and engineering capacityDefine initiative scope and success criteria, including problem statements, target users, KPIs, and release metricsDevelop clear, actionable product requirements (PRDs, epics, user stories, and acceptance criteria) to enable efficient deliveryPartner with engineering, design, and data/analytics teams to drive agile delivery while proactively managing dependencies, risks, and trade-offsLeverage customer feedback, product analytics, and market insights to inform prioritization and continuous improvementCollaborate with commercial, business development, and strategy teams to ensure solutions are differentiated and aligned to market needsSupport go-to-market readiness by contributing to positioning, demos, release materials, and sales enablement assetsCommunicate product status, priorities, and decision rationale clearly to stakeholders to ensure transparency and alignmentEnsure delivered capabilities demonstrate measurable business value, driving adoption, workflow impact, and customer outcomesQualificationsBachelor’s degree required; Master’s preferred (Computer Science, Healthcare, Business, or related field), or equivalent experience5+ years of product management experience, preferably in software, data, or analytics-driven productsExperience working with healthcare provider organizations, business development, and/or strategy teamsStrong data-driven decision-making capabilities, including use of KPIs, analytics, and customer/market insightsDemonstrated ability to lead cross-functional delivery and influence without direct authorityExperience working in Agile/Scrum environments with tools such as Jira, Confluence, or similarExcellent written and verbal communication skills, with the ability to engage both technical and executive stakeholdersPreferred QualificationsExperience in healthcare analytics, provider solutions, or commercial strategy productsFamiliarity with PRM, referral optimization, territory planning, or resource allocation workflowsExperience supporting go-to-market launches and sales enablement initiativesThis is a remote/WFH position open to candidates currently residing within the United States. 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 $98,500.00 - $274,400.00. 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.

BIOAXIS Healthcare, an IQVIA company and the largest organization specializing in high‑level patient education and care services through patient support programs, is seeking on behalf of a client, a multinational pharmaceutical company, a Pharmacy Sales Representative. Responsibilities Conduct daily visits to pharmacies to provide information and promote pharmaceutical productsProvide clear, accurate scientific informationGather insights and data from pharmacies and the marketSupport promotional and communication activities Qualifications Previous experience as a pharmacy representative, medical sales representative, or relevant experience in the healthcare sectorCar driving license and ability to travel Skills Excellent communication and presentation skillsΟrganizational mindset, consistency, and professionalismIQVIA 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 Summary This position provides hands-on experience in the preparation, documentation, and management of investigational products for clinical trials. The intern will work under the direct supervision of a licensed pharmacist to support study start-up, dispensing, inventory, and documentation processes, while gaining exposure to community-engaged clinical research. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Study Start-Up & Documentation:• Assist in the development, preparation, and maintenance of protocol-specific documents, including:• Compounding worksheets• Drug accountability logs• Patient medication diaries• Dosing instructions• Visit-specific medication handouts or counseling sheets• Format and print protocol materials for staff and participants; maintain document version control.• Support setup of study binders, electronic files, and documentation templates for each trial. Dispensing & Inventory:• Assist in the preparation, labeling, and dispensing of investigational drugs per protocol and Good Clinical Practice (GCP) guidelines.• Help manage inventory tracking, including receiving study drug shipments, logging lot numbers, expiration dates, and storage conditions.• Monitor refrigerator/freezer logs and report temperature excursions promptly.• Reconcile drug inventory and assist with preparing drug return or destruction forms. Participant & Study Support:• Provide study participants with protocol-specific medication instructions and review diary completion processes under pharmacist supervision.• Communicate with clinical coordinators and nurses regarding drug availability and dosing schedules.• Assist in packaging take-home medication kits for participants in compliance with study requirements. Regulatory Compliance:• Maintain accurate, real-time documentation for investigational drug accountability.• Support compliance with FDA, IRB, sponsor, and Virginia Board of Pharmacy regulations.• Participate in internal audits and assist with documentation for sponsor monitoring visits. Knowledge Skills and Abilities • Strong written and verbal communication skills.• Excellent attention to detail and documentation accuracy.• Interest in community-based clinical research, public health, or investigational drug services.• Proficient with Microsoft Word, Excel, and PDF editing tools for document preparation.• Ability to work independently and collaboratively in a small, mission-driven team environment. Required Education and Experience Education: • Currently enrolled in an ACPE-accredited PharmD program. • Must be in good academic standing and eligible for internship experience in a clinical research setting. · Current IV Certification (required)  Licensure:  · Current Pharmacy Intern License (required) in the state where the NEXT Oncology position is located. Preferred Qualifications:• Previous experience in a pharmacy, research, or clinical setting.• Familiarity with clinical trial operations, GCP, or IND processes.• Coursework or interests related to pharmacotherapy, research ethics, or public health. Learning and Development Opportunities • Experience supporting real-world, community-focused clinical trials.• Hands-on exposure to investigational drug handling, documentation, and regulatory  compliance.• Opportunity to contribute to health equity and translational research efforts in underserved populations.• Mentorship and training by clinical research pharmacists and study staff 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 $33,000.00 - $82,600.00. 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.

Account Manager, Inside SalesJob OverviewIQVIA is seeking an Inside Sales Account Manager to support growth across our Emerging Biopharma and Pre-Commercial portfolios. This role identifies, engages, and qualifies prospective clients across small, emerging, and clinical-stage biopharma companies as they advance assets through development, launch preparation, and commercialization planning.The Business Development Representative will partner with Business Development, Account Management, Marketing, and solution teams to generate qualified opportunities, support pipeline development, and connect clients with IQVIA’s data, analytics, consulting, real-world evidence, market access, medical affairs, launch, and commercialization capabilities.Essential Functions• Identify, research, and qualify new sales opportunities within assigned Emerging Biopharma and Pre-Commercial target accounts.• Conduct proactive outbound outreach through phone, email, digital sales tools, and CRM-supported campaigns.• Engage prospects in discovery conversations to understand business priorities, buying needs, timelines, and fit for IQVIA solutions.• Monitor account, pipeline, funding, clinical, and market signals to inform targeted outreach and sales prioritization.• Partner with Business Development, Account Management, Marketing, and Go-To-Market teams to support account planning and lead conversion.• Coordinate qualified leads and next steps with field sales and portfolio leads to ensure timely follow-up and a consistent customer experience.• Maintain accurate CRM documentation of activities, contacts, account intelligence, opportunity status, and follow-up actions.• Track outreach activity, lead conversion, and pipeline contribution; provide regular updates to sales leadership and internal stakeholders.• Support preparation of call plans, account briefs, client materials, and internal opportunity summaries.• Build effective relationships across sales, marketing, solution specialists, consulting, analytics, and delivery teams.• Maintain knowledge of IQVIA offerings, Emerging Biopharma market dynamics, Pre-Commercial priorities, and relevant life sciences trends.Qualifications• Bachelor’s degree in business, life sciences, healthcare, marketing, communications, or related field preferred; equivalent combination of education, training, and experience will be considered.• 3+ years of relevant inside sales, business development, lead generation, account development, customer engagement, or life sciences commercial experience required.• Experience in healthcare, pharmaceutical, biotech, life sciences services, data/analytics, consulting, or commercialization solutions strongly preferred.• Demonstrated ability to prospect, qualify leads, conduct discovery, and manage follow-up activity in a disciplined manner.• Strong verbal and written communication skills with the ability to tailor messaging to customer needs.• Ability to synthesize account research, market signals, and customer information into clear outreach strategies.• Comfortable working in a fast-paced, matrixed environment with multiple stakeholders and priorities.• Strong attention to detail, organizational skills, CRM discipline, and proficiency with Microsoft Office and digital sales engagement tools.• Positive, proactive, collaborative, and customer-focused approach with a commitment to achieving lead generation and pipeline contribution goals. Please Note: You must reside within the country where this role is posted in order to be eligible for this remote position. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $54,300.00 - $135,700.00. 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.

LocationOffice-based in Fairfax, VA  Job Summary The Phlebotomist will obtain and prepare specimens for analysis and perform various screening tests. Provide basic medical care to patients under the supervision of RNs/Physicians. Advocates for patient safety and protocol integrity, adheres to standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.  Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Obtains, and documents vital signs to include pulse, blood pressure, temperature, respiratory rate, height, and weight Confirms and documents fasting status Obtains and documents pain scale and fatigue scale Obtains clinical labs and study specific specimens according to the patients schedule and protocol guidelines Obtains good quality ECGs according to the patients schedule and protocol guidelines Assists RNs/Physicians with procedures or examinations Prepares laboratory requisitions and supplies Maintains cleanliness of draw stations and work areas Inventories and requests supplies as necessary Other duties as assigned Required Education and Experience High school diploma or equivalent Current BLS required MA certification OR Phlebotomy certification required Previous experience in a health-related field preferred Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. 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 $25,900.00 - $64,800.00. 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.

Site Enrolment & Engagement Lead 12-month fixed term contract. Open to all locations across Australia. About the role We are looking for a Site Enrolment & Engagement Lead to support clinical research sites with patient recruitment, retention and study-specific education. This is an excellent opportunity for someone who wants exposure to clinical research, and enjoys working closely with sites and healthcare professionals to improve trial delivery. The therapeutic area this role will focus on is Pulmonary Arterial Hypertension (PAH) and Idiopathic Pulmonary Fibrosis (IPF). In this role, you will work in partnership with research sites, investigators and internal teams, acting as a trusted point of contact for trial-related education, site engagement and recruitment support. As you build experience, your responsibilities and level of autonomy will grow. What you’ll be doing: Partnering with clinical research sites to develop study-specific action plans that support patient recruitment, retention and study delivery Providing education and training to healthcare professionals and site staff on clinical trial protocols, procedures and study requirements Supporting study-specific training needs, helping sites understand and implement trial processes effectively Identifying and helping address recruitment and retention barriers, sharing best practice and practical solutions Working with referral networks where appropriate to help identify potential trial participants In some studies, interacting directly with patients to provide education on the trial, disease area, or device/medication (where required and appropriate) Analysing site activity and engagement data to help tailor strategies that maximise pre-screening, screening and enrolment Accurately completing internal reporting and documentation Organising or supporting group meetings, site visits and educational sessions Maintaining up-to-date knowledge of relevant therapeutic areas and disease states Managing queries or objections from site staff in a professional, solution-focused way Looking after company equipment and following all compliance and safety requirements About you: A bachelor’s degree in health sciences or a related field Active license or credential in one of the following: MD – Medical Doctor DO – Doctor of Osteopathic Medicine RN – Registered Nurse NP – Nurse Practitioner PA – Physician Assistant Pharmacist – RPh or PharmD Occupational Therapist Physical Therapist Respiratory Therapist Pulmonary Arterial Hypertension (PAH) and Idiopathic Pulmonary Fibrosis (IPF) therapeutic area experience essential Experience in a Clinical Trial Educator / Site Engagement & Enrolment position or similar role within clinical research / studies Strong communication and interpersonal skills, with the ability to build rapport quickly A collaborative, customer-focused mindset and a genuine interest in clinical research The ability to work independently while knowing when to ask for support Good organisational skills and attention to detail A proactive, solutions-oriented approach to problem solving Flexibility to travel as required for site visits Cultural awareness, empathy and professionalism when working with diverse patients and site teams Why join us? Structured onboarding and ongoing training Exposure to a wide range of clinical research stakeholders and therapeutic areas Clear opportunities to grow and develop within the Site Engagement & Enrolment Lead career path A collaborative, supportive team environment Meaningful work that helps improve patient access to clinical trials If you are interested please apply with your resume. If you are successful you will receive an email to complete an online assessment. Candidates who pass this assessment will be contacted direct by the IQVIA Recruiter to discuss. 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.

Essential Functions: TMF: Set up and maintain the site level TMF/eTMF, coordinate on document collection, uploading into SharePoint (SP)/eTMF, check the document completeness, and provide TMF/eTMF quality control (QC) if required. EC Submission: Coordinate on EC submission dossier, site start-up preparation, and EC fee application and tracking. Process protocol amendments; may include ICF updates. Tracker/Metrics Report: Collect and update study trackers/metrics report for site level if needed. Site Contract and Payment: Assist in contract signature process; assist in site level payment initiative and payment and invoice tracking. Site Materials and Equipment: Distribute site materials and equipment, document printing, shipment, and other administrative work. Administrative: Business and department office administration support if required. To undertake other reasonably related duties as may be assigned from time to time, as appropriate for level of experience Job Requirements: Bachelors Degree in Pharmaceutical or related field Minimum 0.5 years of clinical trial experience in the pharmaceutical or CRO industry. Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Broad knowledge of applicable protocol requirements as provided in company training Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint Good written and verbal communication skills including good command of English language Excellent organizational skills and ability to prioritize and multitask 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 Overview Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget. The Clinical Project Manager leads the regional clinical operations team (including oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study. Ensures alignment of regional deliverables with overall study goals. Essential Functions Leads the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study Leads external vendors involved in study delivery on a regional level Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Project Manager as required Represents the regional project team at internal meetings and at the cross-functional Clinical Project Team (CPT) meetings Leads regional operations meetings with all regional project team members Leads planning and management of the assigned clinical projects from feasibility through closeout activities for region, in line with global project timelines Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these Ensures that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders  Provides regional input on global study plans as required Ensures timely availability of local adaptations of global study documents such as informed consent forms, in close collaboration with other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs Accountable for submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs Ensures regional and country information in study systems and tools is entered and up to date Collaborates closely with CRAs in the region to ensure proper study execution at the sites. Reviews and signs-off monitoring reports Responsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QC’d on a regular basis as per the study TMF QC plan Provides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region. Provides input on local regulatory approval and reimbursement status of comparator drugs used in study for countries in region Manages the trial data collection process for the region, drives data entry and query resolution As required, supports planning and execution of the Clinical Study Report in collaboration with Global Clinical Project Manager and Medical Writing Handles escalated issues or problems with the sites in region in close collaboration with stakeholders such as country heads Monitors study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulations Ensures inspection readiness for study in region at any point in time throughout the study life cycle Informs Global Clinical Project Manager of any issues arising on the study, evaluates impact and ensures solutions are implemented Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate Collaborates with CPT members and colleagues to ensure cross-team, site learnings, and best practices are shared Leads improvements and partners with CPT members to enhance the efficiency and the quality of the work performed on assigned studies Contributes to development, optimization and review of work instructions and SOPs as required Works with the sourcing team to select and manage regional study vendors Manages regional study budgets Works closely with Clinical Business Operation on investigator fees, site payment issues and patient travel reimbursement activities Identifies and manages regional team resource needs and establishes contingency plans for key resources Monitors regional resource utilization over study life cycle and liaises with functional managers as needed Qualifications Bachelor's Degree Life sciences or related field Progressive experience in clinical research within biotech, pharma or CRO industry 7 years of monitoring experience including > 1 years project management experience or equivalent combination of education, training and experience. Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Communication - Strong written and verbal communication skills including good command of English language. Strong presentation 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.

Job OverviewResponsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process.  Essential Functions• Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects.• 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 Analysts, Consultants, and where relevant, to Statistical Services assigned to engagement.• Develops detailed documentation and specifications.• Performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client specific solutions.• Designs, structures and delivers client reports and presentations that are appropriate to the characteristics or needs of the audience.• May deliver some findings to clients.• Recommends improvements and alternative solutions to resolve problems.• 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 methodologies and life sciences market through on the job experience and participation in training opportunities. Begins to develop CoE specific subject matter expertise.• When acting as Project Manager, proactively manages project timelines and manages day to day communication with the client and team members.Qualifications• Bachelor's Degree required.• Master's Degree Business Administration preferred.• 5-8 years of related experience in consulting and/or life sciences industry required.• Possesses solid project management skills and client influencing and relationship building skills.• Works willingly and effectively with others in and across the organization to accomplish team goals.• Experienced with developing consultative relationships with senior level managers and executives at clients in the life science industry.• Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.• Knowledge of consulting methodologies, tools and techniques related to functional area.• Knowledge of key issues and current developments in the life science industry.• Excellent presentation, communication and client influencing skills.• Has established network and referral contacts.• Has necessary subject matter expertise to effectively manage projects within a given CoE. 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.

We are seeking Project Delivery Manager to join IQVIA Laboratories at Valencia, CA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Lead and support the Client Delivery Team to achieve client and company goals while ensuring high-quality project execution and service delivery. This fully remote role provides day-to-day leadership, supports occasional early meetings based on time zone and global meeting needs, and may require limited travel or onsite attendance for specific client meetings or audits. What You'll Be Doing:Lead and manage the day-to-day activities of assigned staff in line with organizational policies and applicable regulationsMentor, train, and develop team members while supporting performance management and professional growthBuild strong client relationships and serve as a liaison between sponsors, internal departments, external vendors, and project teamsEnsure studies are planned and executed in accordance with FDA, ICH, and/or EMEA guidelines and Good Clinical PracticeReport team productivity, quality, and performance metrics against contract, client expectations, and project baselines to managementParticipate in customer meetings, bid defense activities, and employee engagement initiatives that support operational successSupport a fully remote working model with flexibility for occasional early meetings, limited travel up to four times per year, and onsite attendance for specific client meetings or audits when needed What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferredMinimum 4 years of experience in clinical trials/ hospital-funded research, project management or laboratory environmentDemonstrated computer proficiency with Microsoft Office and the company systems, or equivalent experience with similar Centralized Laboratory systems preferredStrong knowledge of Project Services processes, the company laboratory processes, and/or equivalent working knowledge of central laboratory operations preferredOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong people management skills with the ability to develop and lead cross-functional teamsExcellent interpersonal, organizational, and client management skillsDemonstrated ability to work in a fast-paced environment, meet deadlines, and communicate effectively in EnglishAbility to establish and maintain effective working relationships with coworkers, managers, and clients What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit IQVIA Benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary 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 $80,200.00 - $167,200.00. 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.