Clinical Project Manager, Immuno-Oncology - IQVIA Biotech
$93.1k - $232.8kIQVIA
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a US-based Clinical Project Manager with proven experience in Immuno-oncology and Cell & Gene Therapy clinical trials to join IQVIA Biotech.OverviewAs a Clinical Project Manager, you’ll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will serve as a key member of the core project team, ensuring the successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role blends strategic leadership, operational excellence, financial oversight, and customer partnership to drive high‑quality outcomes across regional and global studies.Key ResponsibilitiesParticipate in bid defense presentations and contribute to study strategy development; may lead presentations for smaller or regional studies.Develop and implement integrated study management plans alongside the core project team.Lead the planning and execution of smaller or less complex regional clinical studies, optimizing speed, quality, and cost.Serve as a primary or backup point of contact for clients, fostering strong, collaborative customer relationships.Build, manage, and guide cross‑functional project teams, ensuring effective communication and milestone achievement.Monitor study progress, proactively manage risks, and drive timely issue resolution.Ensure adherence to ICH GCP, applicable local regulations, standard processes, and company policies.Manage project financials, including forecasting, scope management, revenue optimization, and identification of acceleration opportunities.Oversee vendor management activities when assigned.Support team development by mentoring less experienced project team members and contributing to a culture of continuous improvement.QualificationsBachelor’s degree in Life Sciences or a related field.5+ years of relevant clinical research experience, including at least 1 year of project management experience.Broad protocol and therapeutic knowledge; familiarity with the competitive landscape and ability to articulate the value of IQVIA solutions.Excellent communication and presentation skillsProven leadership capabilities, including decision‑making, performance management, and cross‑functional collaboration.Strong problem‑solving, planning, organizational, and prioritization skills.Ability to manage conflicting priorities while maintaining quality and accuracy.Proficiency in MS Office applications (Word, Excel, PowerPoint).Understanding of project financials, including budgets, forecasting, and contractual obligations.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 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. 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 $93,100.00 - $232,800.00. 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.SummaryLocation: Durham, North Carolina, United States of AmericaType: Full time
$93.1k - $232.8k
Job OverviewIQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE... ...observational studies within the oncology therapeutic area. It is important for... ...Therapeutic area expertise desired (oncology)IQVIA is a leading global provider of...SuggestedFull timePart timeImmediate startWorldwide$93.1k - $232.8k
Job OverviewSenior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve... ...and practices. Clinical Project Management is focused on project delivery,... ...therapeutic expertise and IQVIA’s suite of solutions to drive operational...SuggestedFull timeContract workPart timeImmediate startWorldwide$93.1k - $232.8k
Job SummaryThe Project Lead is responsible for ensuring that all studies... ...CROs.Collaborating across Clinical Operations and other... ...including > 1 year’s project management experience.Conceptual and practical... ...Operations or related areas.IQVIA is a leading global provider...SuggestedFull timeTemporary workPart timeImmediate startWorldwide- ...Clinical Research Coordinator, Senior - Duke Cancer Institute Work Arrangement: On-Site... ..., and multiple affiliations. Be You The Oncology Clinical Research Unit (CRU) within the... ...supervise a team of study coordinators and data managers/coordinators as part of your leadership...SuggestedTemporary work
$64.97k - $105k
...Duke Cancer Institute (DCI) is seeking a Clinical Research Nurse Coordinator to join our... ...hands-on coordination for multiple, complex oncology clinical trials, including studies... ...organizational skills with the ability to manage multiple, complex clinical trials...SuggestedFull timeWork experience placement- ...Duke Cancer Institute's Oncology Clinical Research Unit seeks a Senior Clinical Research Coordinator to lead complex leukemia/MPN trials. You will supervise coordinators and data managers, partner with PIs, and drive enrollment and regulatory compliance across multiple...
$59.83k - $99.96k
...Clinical Research Coordinator - Duke Cancer Institute Work Arrangement: Hybrid (On-Site... ...patient care and outcomes in neuro-oncology. You will serve as a central leader and... ...experience Experience with clinical data management systems and electronic medical records (...ApprenticeshipWork at officeRemote work$64.97k - $105k
...Clinical Research Nurse Coordinator - Duke Cancer Institute Work... ...successful execution of complex oncology clinical trials within the... ...teams to recruit, enroll, and manage study participants. You will... ...supporting team development and project completion Participate in...Temporary workWork experience placement$64.97k - $105k
...Clinical Research Nurse Coordinator - Duke Cancer Institute Work Arrangement: On-Site... ...clinical nursing expertise with leadership in oncology research to support innovative clinical... ...Center). Be Bold. Coordinate and manage oncology clinical trials by supporting...Work experience placementWork at office- ...Our FSO team is seeking an Cell & Gene Therapy Sr. Clinical Project Manager to join our growing team. This role requires 4+ years of global project management experience , with mandatory experience in cell & Gen . Candidates must be based in the United States . Job Overview...Full timeContract workPart timeWork at officeFlexible hours
- Responsibilities Coordinate and manage oncology clinical trials by recruiting, screening, consenting, and enrolling participants while ensuring adherence to study protocols and regulatory requirements Deliver direct patient care in a research setting, including medication...
$57 - $71.32 per hour
...Job Description Job Title: Contract Clinical Study Manager Job Description The Contract Clinical... .... Coordinate closely with internal project team members, CROs, vendors, investigators... ...location provides access to a vibrant biotech ecosystem, a strong talent network,...Contract workTemporary workWork at officeMonday to FridayDay shift3 days per week$95k - $175.7k
Description Clinical Project Manager II - Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA Preferred)Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators...Contract workImmediate startRemote workFlexible hours- ...A leading biopharmaceutical solutions organization in Morrisville, NC is seeking a Project Manager to support the management of clinical studies. The role involves coordinating study deliverables, managing vendor relationships, and developing risk mitigation strategies...
$95k - $175.7k
Clinical Project Manager II – Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success...Contract workRemote workFlexible hours2 days per week3 days per week- ...Requirement/Must Have: 1+ years of relevant work experience in a clinical environment or medical setting. High school diploma (A BS... ...planning related to staffing and scheduling for research projects. Skills: Knowledge of clinical trials and departmental, protocol...Work experience placement
- ...Clinical Laboratory Supervisor The Clinical Laboratory Supervisor is responsible for overseeing the day‑to‑day testing activities in... ...high complexity molecular testing within global clinical trials, management of scientific staff and accurate reporting of test results...Temporary workShift work
$53.56k - $61k
...and research.Patient care: We promote health and provide superb clinical care while maintaining our strong tradition of reaching... ...Clinical Research Data Coordinator is responsible for research data management for a variety of complex clinical research protocols,...Permanent employmentFull timePart timeLive inWork at officeLocal areaWeekend workAfternoon shift- ...Clinical Research Nurse Coordinator Work Arrangement: Regular Location: Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER School... ...activities, etc.), and will work with the Division Lead to manage regulatory tasks (such as study start up and close out, IRB tasks...Flexible hours
- ...University of North Carolina at Chapel Hill seeks a Clinical Research Coordinator within the Center for Gastrointestinal Biology and... ...GI-focused clinical studies, independently collect data, manage project tasks, and communicate with diverse stakeholders. The role emphasizes...
- ...Clinical Research Coordinator Location: Chapel Hill, NC 27516 (Hybrid) Duration: 3 Months Required: Bachelors Degree Specialized... ...role in implementing changes in design of clinical research management. Ability to problem solve and resolve quality control issues...Work at officeWeekend work
$70k - $84k
...Position Type: Permanent Staff (EHRA NF) Working Title: Senior Clinical Research Coordinator Appointment Type: EHRA Non-Faculty Research... ...and maintain effective working relationships with coworkers, managers, and clients. Ability to manage competing priorities, including...Permanent employmentFull timePart timeLive inWork at officeLocal areaAfternoon shift2 days per weekEarly shift- ...regulatory compliance test, is currently seeking candidates for a Lab Manager position. The successful candidate will possess a strong work... ..., results, and compliance pathways. Support Sales and Project Management teams by providing technical input during quoting, test...
- ...environment and wear appropriate personal protective equipmentMinimum QualificationsBachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology1 year or more of clinical laboratory testing experience OR an MLS degreePreferred...Temporary workCasual workInternshipFlexible hoursShift work
- ...appropriate personal protective equipment Minimum Qualifications ~ Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology Preferred Qualifications ~3 months or more of clinical laboratory testing experience...Temporary workTraineeshipCasual workInternshipFlexible hoursShift work
- ...community. No matter where your talents lie, join us and discover how we can advance health together. Duke University Health System Clinical Laboratories Pursue your passion for caring and innovation as a team member in the state-of-the-art Duke Health laboratories....Monday to FridayWeekend workAfternoon shift
- ...can advance health together. Duke University Health System Clinical Laboratories Pursue your passion for caring and innovation... ...procedures and policies for accuracy and submit changes to the manager or designee. Understand, comply, and perform all necessary...Monday to FridayAfternoon shift
$26 - $45 per hour
...variety of patient tests and provide administrative support for clinical operations within the healthcare facility Perform blood... ...Identification, DAT, Eluate, Phenotyping, and Antigen Typing Manage product modifications including syringe aliquots and...Hourly payPermanent employmentFull timeRelocation packageShift work- MT/MLT opening at a very highly ranked hospital near Oak Grove, NC with 354 staffed beds. Those hired will as a full-time Core Lab Generalist. Shift: Monday to Friday, 3rd shift, (11p 7:30a) ASCP (or equivalent) required This is a permanent, full-time position...Permanent employmentFull timeMonday to FridayShift workNight shift
- ...wear appropriate personal protective equipment Minimum Qualifications ~ Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology ~1 year or more of clinical laboratory testing experience OR an MLS degree...Temporary workCasual workInternshipFlexible hoursShift work
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