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. US‑based Clinical Project Manager with proven experience in Immuno‑oncology and Cell & Gene Therapy clinical trials is needed to join IQVIA Biotech. Overview As a Clinical Project Manager, you’ll play an essential role in accelerating clinical trial delivery and improving patient lives by bringing 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 Responsibilities Participate 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. Qualifications Bachelor’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 skills. Proven 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. 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. 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. #J-18808-Ljbffr IQVIA
$93.1k - $232.8k
...Clinical Project Manager IQVIA Biotech is seeking a Clinical Project Manager with oncology experience. Job Overview: Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the...SuggestedFull timeContract workPart timeLocal areaWorldwide$93.1k - $232.8k
...IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically...SuggestedFull timePart timeImmediate start$93.1k - $232.8k
Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment... ...of real‑world observational studies within the oncology therapeutic area. It is important for this individual...SuggestedFull timePart time$93.1k - $232.8k
Job Overview Senior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to... ...policies and practices. Clinical Project Management is focused on project delivery,... ...therapeutic expertise and IQVIA’s suite of solutions to drive operational...SuggestedFull timeContract workPart timeLocal areaImmediate start$93.1k - $232.8k
...candidates with: 2 years of clinical trial management experience (preferably at CRO) 2 years of oncology experience required (phase I,... ...Lead is a member of the core project team responsible for the... ...influence without authority. IQVIA Core Competencies - Ability to...SuggestedFull timeContract workPart timeWork at officeLocal areaWorldwide$125k - $135k
Job Overview Project Managers own the operational strategy, determining the most cost effective... ...innovation and future focused approaches to clinical trials with a focus on patient... ...Therapy studies Experience working with Biotech clients In lieu of the above requirement...Full timeContract workPart timeWork at officeLocal areaRemote workFlexible hoursNight shift$59.83k - $99.96k
...Clinical Research Coordinator - Duke Cancer Institute Work Arrangement... ...is housed within the Oncology Clinical Research Unit (CRU)... ...standardized scripts Experience managing complex operational tracking... ...meet and maintain Duke and project-specific training and certification...ApprenticeshipWork experience placementWork at officeRemote work$93.1k - $232.8k
## Clinical Project Manager- IVDApplylocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Todayjob... ...and basic knowledge of Clinical Operations or related areas.IQVIA is a leading global provider of clinical research services,...Full timeTemporary workPart timeImmediate startWorldwide- IQVIA is seeking a Sr. Clinical Project Manager in Durham, North Carolina. The role involves leading the delivery of clinical trials and managing cross-functional teams to improve patient outcomes. It requires over 7 years of clinical research experience, including at least...
$57 - $71.32 per hour
...Job Description Job Title: Contract Clinical Study Manager Job Description The Contract Clinical... ...-out. Coordinate with internal project team members, CROs, vendors, investigators... ...learning, and engage with the broader biotech ecosystem of the Research Triangle...Contract workTemporary workWork at officeRemote workMonday to FridayDay shift3 days per week$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 simultaneously...Work experience placement$64.97k - $105k
Clinical Research Nurse Coordinator - Duke Cancer Institute Work Arrangement: On-Site Requisition... ...Nurse Coordinator to join our dynamic Oncology Clinical Research Unit (CRU). In this... ...will also collaborate with sponsors, manage study operations, and contribute to the...Temporary work$120k - $135k
Clinical Project Manager - Oncology (Client Dedicated/Remote) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization... ...-phase oncology studies (Phase I/Ib) Experience with immuno-oncology, targeted therapies, cell therapy, or hematologic...Contract workWork at officeImmediate startRemote workWorldwideFlexible hours- ...Aerogen Pharma is a US-based clinical-stage specialty pharmaceutical... ...the role? The Clinical Trial Manager (CTM) is responsible for... ...leadership, effective communication, project management skills, and a deep... ...operations role within biotech, pharmaceutical, academic, and...Interim roleWork at office
- CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION North Carolina Department of Health and Human Services requires the services of an EXPERT Epic Clinical project manager to manage the planning and implementation of an EHR implementation project for the Division...
- CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION The North Carolina Department of Health and Human Services requires an expert Epic Clinical Project Manager to oversee the planning and implementation of an electronic health records (EHR) project for the...
- ...preventive health care, at-home tests, or access to lifesaving clinical studies, we aim to provide the necessary resources to... ...Health is seeking a highly skilled and experienced Clinical Project Manager to join our company. In this role, you will be responsible for...Flexible hours
$64.97k - $105k
Duke University’s Center for Cancer Research is hiring a Clinical Research Nurse Coordinator to oversee complex oncology clinical trials. The role requires an RN license in North Carolina and experience in clinical nursing. The ideal candidate will ensure regulatory compliance...- ...Job Title: Clinical Research Coordinator Location: Loma Linda, CA Duration: 9 Months Pay Rate: $36-$38/hr on W2 Timing... ...and perform assigned study procedures. Collect, record, and manage research data, ensuring accuracy and completeness. Prepare...
$59.83k - $99.96k
...Clinical Research Coordinator Work Arrangement: On-Site Location: Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER School... ...specimens and train others in these tasks. Assist with management of IP. Employ the required system for handling, dispensing and...ApprenticeshipWork experience placementWork at office$72.3k - $97.8k
...Clinical Research Coordinator III (CRC3) Organization: The Institute for Medical Research (IMR), an affiliate of the Durham VA Health... ...This is a patient-facing role. This incumbent's first-level manager is the Research Program Manager; the second-level manager is...Full timeContract workFor contractorsWork at officeLocal area$72.3k - $97.8k
...Clinical Research Coordinator III (CRC3) Organization: The Institute for Medical Research (IMR), an affiliate of the Durham VA Health... ...staffing, scheduling, and operational needs Develop, implement, and manage study procedures Identify, screen, recruit, and consent...Full timeFor contractorsLocal area- ...Duration: 12+ Months Manages clinical trial studies for specific therapeutic area(s). Provides guidance and oversight to internal and external project team members for the successful management of all aspects of study operation management in accordance with GCP/ICH Guidelines...Contract workWork at officeRemote work
$59.83k - $99.96k
...Duke PF is seeking a Clinical Research Coordinator for the Duke Cancer Institute in Durham, NC. In this hybrid position, you'll manage study operations, recruit participants, ensure regulatory compliance, and act as a liaison among stakeholders. Qualifications include...$61.03k - $101.96k
...You. This position will serve as the primary coordinator for clinical studies in the Division of Hematology. As the Clinical Research... ...activities, etc.), and will work with the lead coordinator to manage regulatory tasks (such as study start up and close out, IRB tasks...ApprenticeshipWork experience placementWork at officeFlexible hours$59.83k - $99.96k
...Collaborative for Health Justice seeks a Clinical Research Coordinator to co-lead all... ...related agreements are required for their project (examples: independent contractor agreements... ...will take a leadership role in managing project meetings for the Duke site as well...For contractorsWork experience placementLive inWorldwide- A leading clinical research organization in Durham, North Carolina, is seeking a Senior Clinical Research Specialist to support oncology clinical trials. The role involves overseeing study operations, ensuring data quality, and maintaining compliance with regulatory standards...
$20.76 - $31.44 per hour
Clinical Research Specialist, Senior - Duke Cancer Institute Work Arrangement... ..., data collection and management, regulatory documentation,... ...coordination under the oversight of the Oncology Clinical Research Unit (CRU).... ...development, and research project coordination. Other...ApprenticeshipRemote work- ...Summary The Duke Cancer Institute's Thoracic Clinical Research Program is looking for a Senior... ...Research Specialist to join the Oncology Clinical Research Unit (CRU). In this role... ...study operations, study startup, and site management Screen participants for eligibility and...Work experience placement
$20.76 - $31.44 per hour
Duke PF's Cancer Institute in Durham, NC is seeking a Senior Clinical Research Specialist to join its team. This hybrid position involves... ...research studies, including patient recruitment and data management. Candidates should have at least one year of relevant experience...Hourly pay
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