Clinical Project Manager, Internal Medicine, IQVIA Biotech
$93.1k - $232.8kAvery Healthcare Group Ltd.
Clinical Project ManagerIQVIA 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.IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine. As a Project Manager, you'll drive operational excellence, manage cross-functional teams, and ensure high-quality delivery that accelerates life-changing therapies to market.Key Responsibilities:Lead global/regional clinical trials from start-up through close-out.Develop and execute study management plans aligned with contract and strategy.Manage timelines, budgets, and risk mitigation across projects.Serve as the primary contact for sponsors and vendors.Ensure compliance with ICH-GCP and regulatory standards.Mentor and support project team members.Qualifications:Bachelor's degree in Life Sciences or related field preferred.Minimum 5 years of clinical research experience, including 1+ year in project management.Strong therapeutic expertise in Internal Medicine.Proven leadership, communication, and problem-solving skills.Solid understanding of project financials and contract management.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.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.
$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... ...corrective and preventative action plans.Collaborate with internal functional groups to support study execution and...SuggestedFull timePart timeImmediate startWorldwide$93.1k - $232.8k
...IQVIA Biotech seeks a Senior Clinical Project Manager to lead end-to-end execution of multi-regional clinical trials in cardiovascular, renal, and metabolic therapeutics. The role involves strategic oversight, cross-functional team leadership, sponsor engagement, and accountability...Suggested$35 - $42 per hour
...Clinical Research Coordinator - Boulder, CO Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and... ..., data entry accuracy, and query management. Please note: This position is not eligible...SuggestedHourly payFull timePart timeWork experience placementImmediate startWorldwide$106.1k - $295.5k
...Associate Clinical Lead DirectorAssociate Clinical Lead... ...a member of the core project team responsible for... ...regulatory requirements (International Conference on... ...risk mitigation plan and manage clinical risks throughout... ...cultural differences.IQVIA Core Competencies - Ability...SuggestedFull timeContract workPart timeWork at officeLocal areaImmediate startWorldwide$68.4k - $232.8k
...WIs, policies, codes of Good Clinical Practice (GCP), local regulatory... ..., contingency and risk management, budget forecasting, and mitigation... ...documentation gaps across projects and drives resolution activities... ...skills as appropriate.IQVIA is a leading global provider...SuggestedFull timePart timeLocal areaImmediate startWorldwideNight shift- ...IQVIA LLC is hiring a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. On-site in Union... ...participants, and maintaining accurate CRFs. Strong data management and communication skills are essential. #J-18808-Ljbffr
- ...IQVIA LLC is seeking a Clinical Research Coordinator to join our on-site team in Boulder, CO. You will perform clinical procedures, recruit and screen patients, and ensure data quality under supervision of a principal investigator. The role requires a Bachelor’s degree...Part time
- ...Details Recruitment/Posting Title: Clinical Research Coordinator I Job... ..., advanced biotechnology and medicine, environmental and... ...will support the execution and management of clinical research studies,... ...if and when appropriate, and internal equity to ensure fair compensation...Full timeSeasonal workWork at officeFlexible hoursShift work
- IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform clinical procedures, recruit and screen patients, and ensure adherence to study protocols and GCP guidelines. Responsibilities include coordinating studies, maintaining...
$146.54k - $189.64k
...Clinical Trials Manager (CTM)At Gilead, we're creating a healthier world for all people. For more than... ...management by coordinating with the internal teams and external partners (including... ...study objectives. The CTM applies strong project management, clinical, and regulatory...Contract workInterim roleWork at office- ...Clinical Research Coordinator II - Clifton, NJ Clifton, New Jersey Iterative Health... ...guidelines. This role is responsible for managing complex studies with minimal oversight... ..., investigators, sponsors, CROs, and internal teams to drive high-quality study execution...Work at officeLocal area
- ...Iterative Health in Clifton, NJ, is seeking a Clinical Research Coordinator II to independently... ...and regulatory compliance. You will manage visit schedules, lead recruitment, and... ...with sponsors, CROs, investigators, and internal teams to drive enrollment and quality study...
- ...educating students, providing clinical care, and conducting research... ..., advanced biotechnology and medicine, environmental and... ...support to the Director, Program Manager and other professional and research... ...and monitoring of departmental projects, ensuring adherence to...Part timeSeasonal workWork at officeShift work
$65k - $78k
...exclusively for the research and clinical trial industry, providing... ...support the successful execution, management, and ongoing operations of... ...the field of cardiovascular medicine. People-First Culture:... ...for sponsors, CROs, IRBs, and internal research teams. Support monitoring...Full timeTemporary workWork at officeRemote work2 days per week3 days per week- Get AI-powered advice on this job and more exclusive features. The Clinical Research Coordinator will oversee the day-to-day operations of clinical trials, ensuring they are conducted ethically and according to protocol. Key Activities Protocol Familiarization : Understanding...Full timeContract work
$68.4k - $232.8k
...IQVIA seeks a Senior Clinical Trial Manager for oncology sponsor-dedicated work across multiple US locations. This role oversees complex trial operations, site selection, recruitment strategy, compliance, and vendor management while serving as the primary operational contact...Local area$55k - $85k
...without the commute into the city? Our client, a fast-growing clinical research network, runs FDA-regulated IDE and post-market... ...Why join ~ Hands-on IDE trials in vascular and endovascular medicine ~ Real ownership of your site and studies ~ Clear path from...Full time- ...Rutgers University in Newark seeks a Clinical Research Coordinator I to support pediatric dentistry and public health research. Under the PI, you will manage studies from start-up through close-out, ensure regulatory compliance, and maintain data integrity across REDCap...
$55k - $60k
...Clinical Research CoordinatorVitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative... ...-sponsored, ECOG, and investigator-initiated studies.Manage trials across multiple oncology disease groups, including GYN,...Full timeTemporary workWork at officeRemote workMonday to Friday1 day per week- ...RWJBarnabas Health in New Jersey is seeking a Research Coordinator at Cooperman Barnabas Medical Center. The role coordinates clinical trials and ensures regulatory compliance under GCP, maintaining accurate documentation and seamless workflow in the research department...
- Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities, ensure protocol compliance... ...will partner with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment...
- Iterative Health in Clifton, NJ, seeks a Clinical Research Coordinator II to run industry-sponsored trials from start-up to closeout with minimal supervision, covering patient recruitment, consent talks, protocol visits, vitals, and data entry. CTMS/EDC proficiency and...
- Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee supporting Phase II-IV oncology interventional trials at a community hospital site in Newark, NJ. This role is ideal for someone with 6-12 months of coordination experience...Full time
$65k - $78k
Vitalief Inc. is looking for a Clinical Research Coordinator (CRC) to support a vascular medical device registry study in Newark, NJ. The... ...$65,000 and $78,000 based on experience. The role includes managing study activities, ensuring compliance, and collaborating with the...- ...University seeks a part-time Clinical Research Coordinator III in the... ...the Rutgers School of Dental Medicine (RSDM). You will support daily operations, coordinate projects, and liaise with multiple... ...relevant field, strong data management skills, and proficiency with...Part timeWork at office
$32 - $50.73 per hour
...00 AM to 5:00 PMDepartment: Clinical Laboratory - Serology GeneralPay... ...evaluation from IERF (International Education Research Foundation... ...and the completion of special projects as assigned.Perform and... ...practice controls as directed by management.Answer questions from...Full timeTemporary workPart timeWork experience placementWork at officeLocal areaFlexible hours$33.81 - $55.81 per hour
...Thursday, 7:00 AM to 3:30 PMDepartment - Clinical Laboratory - Serology GeneralPay range:... ...detailed credential evaluation from IERF (International Education Research Foundation). The... ...department efficiency. Ability to schedule and manage resources to meet department goals....Full timeTemporary workPart timeWork experience placementWork at officeFlexible hours- ...candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated... ...recognized organization (ASCP or AMT). Work Experience: 1 year Clinical experience (high complexity testing) preferred. Minimum of 1...Work experience placement
$33.81 - $55.81 per hour
...Thursday, 7:00 AM to 3:30 PM Department - Clinical Laboratory - Serology General Pay... ...work practice controls as directed by management. Participate in government or... ...detailed credential evaluation from IERF (International Education Research Foundation). The United...Work experience placementWork at officeFlexible hours$34.39 - $49.11 per hour
...to) the scope and responsibilities of the position, the candidate's relevant work experience, education and training, key skills, internal equity, market data, and organizational needs. About Us University Hospital is one of the nation's leading academic medical...Hourly payTemporary workWork experience placementFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Project Manager, Internal Medicine, IQVIA Biotech. Be the first to apply!
- clinical trials manager Parsippany, NJ
- neuroscience clinical research coordinator Parsippany, NJ
- clinical project manager Parsippany, NJ
- clinical research coordinator Parsippany, NJ
- implementation project manager remote Parsippany, NJ
- project finance Parsippany, NJ
- project controls Parsippany, NJ
- special projects Parsippany, NJ
- projects work from home Parsippany, NJ
- project technician Parsippany, NJ



