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Clinical Research Project Manager Jobs in Basking Ridge, NJ

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Key Responsibilities Coordinate and manage clinical research studies in compliance with study ... projects How to Apply Interested candidates can submit their updated resume along with a cover ...

Jerseydigs

Director, Clinical Research, Obesity

Rahway, NJ · On-site

$255K - $402K/yr

... manage clinical development projects * Assist the team in ensuring that appropriate Corporate ... Facilitate collaborations with external researchers around the world * Travel on company business ...

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Clinical Research Project Manager information

See Basking Ridge, NJ salary details

$51.5K

$88.7K

$136K

How much do clinical research project manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for clinical research project manager in Basking Ridge, NJ is $88,660.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,700.00 and $94,300.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are the key skills and qualifications needed to thrive as a clinical research project manager?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What job categories do people searching Clinical Research Project Manager jobs in Basking Ridge, NJ look for?

The top searched job categories for Clinical Research Project Manager jobs in Basking Ridge, NJ are:

What cities near Basking Ridge, NJ are hiring for Clinical Research Project Manager jobs?

Cities near Basking Ridge, NJ with the most Clinical Research Project Manager job openings:

Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Basking Ridge, NJ as of June 2026, with employment types broken down into 81% Full Time, and 19% Part Time. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $88,660 per year, or $42.6 per hour.

Senior Project Manager Clinical Research

Princeton, NJ • On-site

Abbott
See more jobs at Abbottexternal

Full-time

Medical, Life, Retirement

Re-posted 20 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

171st of 547 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution.

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

Our Global Medical & Scientific Affairs Team has an opportunity for a Senior Project Manager, Clinical Research. This role will be located in our Princeton, New Jersey office on site. This role is based in our Abbott Point of Care(APOC) Division. APOC is a global leader in providing critical medical diagnostic and data management products for rapid blood analysis that are intuitive, reliable, and cost-effective. Our i-STAT System is an advanced, portable diagnostic tool that provides real-time, lab-quality results within minutes to accelerate patient-care decision-making. The i-STAT System has the industry's most comprehensive menu of tests in a single, with-patient platform, including tests for blood gases, electrolytes, chemistries, coagulation, hematology, glucose, and cardiac markers. By delivering lab-quality results in minutes, our i-STAT System fosters a collaborative, patient-centered environment while driving improved operational performance.

What You'll Work On

The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination and ensure the efficient execution, monitoring, and reporting of all Scientific Affairs studies. In addition, they will liaise with cross-functional team members including clinical, regulatory, quality, legal, and supply chain, and will be responsible for managing individual study budgets/milestone payments.

In addition:

  • Coordinate end-to-end research study operations for Investigator Sponsored Studies (ISS) and Collaborative Research Studies (CRS), including proposal review, contracts, study start-up, material shipments, budget management, and study closeout.

  • Ensure compliance and audit readiness by maintaining study documentation, conducting investigator/debarment reviews, documenting communications, supporting SOP updates, and maintaining quality system requirements.

  • Manage financial oversight including Fair Market Value assessments, study budgets, invoice processing, milestone payments, forecasting, and financial tracking/reporting.

  • Oversee study logistics and site support by coordinating study supplies, regulatory labeling requirements, site instructions, training documentation, and collaboration with R&D, Clinical, Regulatory, and Scientific Affairs teams.

  • Support Scientific Affairs initiatives including medical education and writing grants, KOL and advisory board contracting, meeting logistics, reporting for review committees, and other activities delegated by Scientific Affairs leadership.

Required Qualifications

  • Bachelor's degree

  • 10+ years of clinical research/medical affairs/project management experience.

  • Knowledge and experience in working with clinical trials including investigator-initiated research and collaborative research studies.

  • Knowledge and experience in oversight of clinical studies, understanding of statistical techniques, tracking clinical studies, and related publications.

  • Understanding of the clinical laboratory, assay/instrument principles involving in vitro diagnostic products.

  • Form and develop long-term strategic and professional relationships; display socially and professionally appropriate behavior.

  • Strong communication skills demonstrated in publications, presentations, etc. including the ability to confidently speak in public, and lead meetings and group discussions.

  • Ability to work independently and in groups.

  • Demonstrates leadership skills, initiative, critical thinking, and problem-solving skills.

  • Strong organization and time management skills

  • Willing and able to travel up to 10 -15% of the time to meet investigators and clinical trial staff.

Preferred Qualifications

  • Advanced degree (Master's, PhD, or MD)

  • Experience with managing publications

  • Experience running clinical trials in international geographies

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

The base pay for this position is

$86,700.00 - $173,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Clinical Affairs / StatisticsDIVISION:APOC Point of CareLOCATION:United States > Princeton : 400 College Road EastADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 15 % of the TimeMEDICAL SURVEILLANCE:YesSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday), Work with human blood or other potentially infectious materials, Work with infectious organisms or known infectious materialsAbbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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