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Clinical Research Project Manager Jobs Jobs (NOW HIRING)

Baylor Scott & White Health

Research Project Mgr

Plano, TX

$66K - $85K/yr

Provides input to the Principal Investigator on clinical and research issues to establish financial ... Ability to manage time-reactive projects. * Knowledge of the beliefs and practices of developing ...

Apex Informatics

Research project manager

Pasadena, CA · On-site

$78K - $99K/yr

N/A Research Project Manager (PM) contractor with experience managing medium to large scale research studies. A research PM with management of direct reports, including performance reviews and hiring ...

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

As of Aug 9, 2026, the average yearly pay for clinical research project manager jobs in the United States is $86,032.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,500.00 and $91,500.00 per year, depending on experience, location, and employer.
What cities are hiring for Clinical Research Project Manager Jobs jobs? Cities with the most Clinical Research Project Manager Jobs job openings:

Nurse Research Project Manager

Touro University

Valhalla, NY

$109K - $136K/yr

Full-time

Re-posted 22 days ago

Touro University rating

5.9

Company rating: 5.9 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

568th of 617 rated colleges and universities

Job description

The Nurse Research Project Manager plays a key role in the administration and coordination of clinical research projects, supports the day-to-day conduct of clinical research and other sponsored projects while performing nursing responsibilities in accordance with protocol requirements. This position provides direct coordination of study visits, ensures regulatory and protocol compliance, manages study documentation, and delivers patient-centered clinical care to research participants. This position plays a key operational role within the department of medicine, assisting with studies from start-up through completion under the guidance of the PI and research leadership.


  • Coordinates assigned clinical studies from initiation through close-out under PI direction
  • Organizes study start-up activities, including feasibility, regulatory submissions, and staff scheduling.
  • Prepares, maintains, and reconciles study documentation such as source notes, case report forms, and regulatory binders.
  • Schedules and conducts participant visits; ensures accurate data capture and protocol adherence.
  • Monitors participant safety, performs follow-up, and reports adverse events promptly.
  • Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging).
  • Assists in IRB submissions, amendments, and continuing reviews.
  • Maintains participant confidentiality and secure handling of study records.
  • Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging).
  • Performs clinical duties per protocol, including biospecimen collection, study-drug administration, EKGs, and other nursing procedures within scope of practice.
  • Provides patient education and informed-consent discussions in coordination with the PI.
  • Collaborates with care teams to integrate study participation with standard clinical treatment.
  • Advocates for participant safety and wellbeing throughout the research process.

Education/Experience:

  • Bachelor of Science in Nursing, required
  • Licenses or certifications:
  • RN-Registered Nurse - DORA - Department of Regulatory Agencies required.
  • BLS-Basic Life Support (BLS/CPR) - AHA - American Heart Association or American Red Cross required.
  • CITI training
  • Prior experience:
  • 1-2 years of clinical research
  • 2 (+) years of Clinical Bedside Nursing
  • Critical Care Experience Preferred

Knowledge/Skills/Abilities

  • Ability to manage project timelines and competing priorities
  • Familiarity with OMB Uniform Guidance and NIH grant policies
  • Strong communication and documentation skills
  • Detail-oriented and capable of navigating complex institutional processes
  • Proficiency in Microsoft Office Suite
  • Knowledge of IRB submission platforms and regulatory databases

Physical demands:

  • Frequent sitting for administrative work
  • Occasional walking and standing in clinical areas
  • Occasional lifting of study materials and files (under 20 lbs)

Environmental demands:

  • In Person office and clinical exposure
  • Potential exposure to patient care settings and biological samples

USD $109,200.00/Yr.
USD $136,500.00/Yr.

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