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Clinical Research Project Manager Jobs (NOW HIRING)

RESEARCH PROJECT MANAGER

Long Beach, CA · On-site

$75K - $96K/yr

Experience: 5+ years of research project management experience in clinical, behavioral, epidemiological, or scientific research Experience managing research protocols and coordinating ...

Research Project Manager

Hanover, NH · On-site

$71K - $91K/yr

Yes Position Purpose The Research Project Manager plans, manages, and executes complex, multiple ... Jacob Borodovsky, Associate Professor of Health Policy & Clinical Practice Department Contact ...

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 ...

Research Project Manager

Evanston, IL · On-site

$68K - $87K/yr

The Research Project Manager, Center for Communicable and Emerging Infectious Diseases for the ... Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP ...

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Clinical Research Project Manager information

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$50K

$86K

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

As of Jul 13, 2026, the average yearly pay for clinical research project manager 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 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 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 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 are the key skills and qualifications needed to thrive as a Clinical Research Project Manager, and why are they important?

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.
More about Clinical Research Project Manager jobs
What cities are hiring for Clinical Research Project Manager jobs? Cities with the most Clinical Research Project Manager job openings:
What are the most commonly searched types of Clinical Research Project jobs? The most popular types of Clinical Research Project jobs are:
What states have the most Clinical Research Project Manager jobs? States with the most job openings for Clinical Research Project Manager jobs include:
Infographic showing various Clinical Research Project Manager job openings in the United States as of July 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $86,032 per year, or $41.4 per hour.
Research Project Manager

$68K - $87K/yr

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Pine Rest Christian Mental Health Services rating

5.3

Company rating: 5.3 out of 10

Based on 18 frontline employees who took The Breakroom Quiz


Job description

Cost Center

643 Research

Scheduled Weekly Hours

20

Work Shift

Shift & Status

Who Are We?

We at Pine Rest believe in the power of healing and that everyone in our community has the right to expert care for mental health and substance use disorders. We are much more than just the third largest non-profit behavioral health system in the country, our 220-acre main campus, and our network of clinical sites across Michigan. We are a tight-knit community of healers who witness the impact of our life-changing work each day.

Each day, we are closing the gaps in access to care. We are innovating through leading-edge research, testing, programs, and treatment modalities that others replicate across the country. Our services include a state-of-the-art psychiatric urgent care center and a soon-to-be-built pediatric behavioral health center, outpatient, inpatient, partial hospitalization (day programs), assessment and testing, residential, addiction treatment and specialty services such as crisis response, employee assistance programs, forensic psychiatry and psychology, and neuromodulation. On-the-job educational programs for nurses, psychologists, advanced practice providers, psychiatrists, and chaplains are equipping the next generation of care providers.

We are passionate about serving and are honored to be a part of this incredible work.

What Will you Do?

As a Research Project Manager at Pine Rest, you'll conduct, monitor, and coordinate the day-to-day activities of assigned research projects, while actively contributing to the quality and improvement of the research program. Key responsibilities include, but are not limited to, developing and maintaining research records, generating reports, recruiting participants, tracking research activities, and analyzing program activity. The Research Project Manager carries out clinical research involving human subjects, ensures compliance with study protocols, adheres to all regulatory requirements, and maintains participant safety, while identifying opportunities to enhance the processes and efficiency of clinical human research studies. This person also engages with industry partners to identify new research opportunities and promote Pine Rest's clinical research capabilities. The Research Project Manager must demonstrate excellent customer service, strong attention to detail, and enthusiasm for the program and the Pine Rest organization.


Principal Duties and Responsibilities:

  • Manages assigned human clinical research studies in psychology and psychiatry conducted at Pine Rest CMHS and Michigan State University College of Human Medicine (MSU-CHM), and in collaboration with academic leaders and industry partners as applicable.
  • Identifies and pursues opportunities for the department to participate in industry-sponsored clinical studies, including outreach to potential sponsors and promoting the organization's research capabilities.
  • Supports evaluation and preparation of research studies for implementation including assessment of operational feasibility; of IRB documents; generation of data collection tools, case report forms; and attends study meetings.
  • Works closely with the Principal Investigator (PI) of each study to implement the study protocol and confer regularly with PI, study team, and Research Department leadership to ensure high quality implementation.
  • Identifies and recruits eligible subjects, screens for eligibility, obtains informed consent, and enrolls participants per protocol.
  • Manages and/or performs the daily study operations, including overseeing study visits, identification of adverse events, compiling, filing and reporting data.
  • Ensures protocol-required assessments are completed for each study participant at designated research visits, including but not limited to physical exams, laboratory work, psychiatric and psychological assessments; with appropriate training and delegation, perform required research activities and procedures in accordance with the study protocol.
  • Assists with the management of investigational product receipt, storage, dispensing, and accountability in accordance with study protocols, sponsor requirements, and regulatory guidelines.
  • Facilitates and/or performs biospecimen collection, processing, transport, and shipping in accordance with study protocols and regulatory requirements.
  • Maintains and reviews study source documentation and regulatory binders, supporting monitoring visits, audits, and regulatory inspections as needed.
  • Maintains research studies in compliance with federal, state, and local law, GCP, contracts, and institutional policies; keeps current with applicable regulations regarding research on human subjects.
  • Facilitates processing and tracking of study-related invoices; collaborates with finance to verify appropriate allocation of costs to the correct study and budget.
  • Promotes research and the Research Department throughout Pine Rest CMHS, and supports continuous enhancement of study processes and operational efficiency in clinical human research within the organization.
  • Supports development and dissemination of research findings, including preparation and submission of manuscripts, abstracts, and related materials.

Supervisory Responsibilities:

  • Project specific study team personnel and contractors.

What Does This Role Require?

  • Bachelors required or Master's degree (preferred) in public health, healthcare administration, project management, or equivalent.
  • Minimum of 5 years of experience in research, specifically human clinical trials are preferred.
  • Minimum of 5 years of successful project management experience.
  • Experience with mental health services is preferred.
  • CITI Human Research Training Certificate and/or Good Clinical Practice Training Certificate is required.

Benefits:

  • Medical, dental, vision & life insurance plans
  • 403(b) retirement match contribution by Pine Rest
  • Generous PTO for full and part time employees
  • Tuition assistance & loan forgiveness
  • Employee Assistance Program offering many free and discounted services for therapy, legal, accounting, gym membership, etc.
  • Partnership with Davenport University provides generous discount on tuition for employees and family members.

Notice:

Pine Rest provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

All new employees are subject to a criminal background check and education verification which may include sending a copy of your high school diploma, GED, or college transcripts.

NOTICE: Successful completion of a drug screen prior to employment is also part of our background process.


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