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Clinical Project Jobs (NOW HIRING)

IQVIA, Inc.

Clinical Project Manager

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own ...

University of Utah

Clinical Project Managers

Campus, IL · On-site

$110 - $150/hr

Priority Review Date (Note - Posting may close at any time) Job Summary Clinical Project Managers This position is patient-sensitive and must fulfill all associated vaccination requirements, or be ...

PSI CRO

Clinical Project Manager

Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in ...

FOCUSKPI INC

Be Seen First

Clinical Project Coordinator

Mountain View, CA · On-site

$30/hr

FocusKPI is seeking a Clinical Project Coordinator to join one of our clients, a high-tech SaaS company. Work Location: Mountain View, CA (Onsite role, 5 days/week) Duration: 6-month contract with ...

PSI CRO

Clinical Project Manager

Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in ...

ICON

Senior Clinical Project Manager

Blue Bell, PA · On-site

Senior Clinical Project Manager - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Collabera

Clinical Project Manager

Santa Clara, CA · On-site

Clinical Research experience in the Medical Device/Pharma industry is a plus. Skills 1) Project Management 2) Business Analysis 3) Business Process Modeling 4) Clinical Technology Strategy 5) User ...

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How much do clinical project jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical project in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What is a clinical project manager?

A Clinical Project Manager is a professional who oversees and coordinates all aspects of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They are responsible for planning, executing, and closing clinical research projects, ensuring that studies are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, collaborating with stakeholders, and handling documentation and reporting throughout the clinical trial process.

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

To thrive as a Clinical Project Manager, you need a background in life sciences, experience in clinical research, and strong project management skills, often supported by a relevant degree and certification such as PMP or equivalent. Familiarity with clinical trial management systems (CTMS), regulatory compliance platforms, and data analysis tools is essential. Exceptional communication, leadership, and problem-solving skills set outstanding Clinical Project Managers apart. These skills and qualifications are crucial for ensuring clinical studies are conducted efficiently, compliantly, and within budget and timelines.

What are some common challenges faced by clinical project managers during multi-site clinical trials?

Clinical project managers often encounter challenges such as coordinating communication between diverse study sites, ensuring protocol compliance, and managing timelines across different geographic regions. Overseeing multiple teams requires strong organizational skills and adaptability, as unexpected issues like patient recruitment delays or regulatory changes can arise. Effective project managers proactively identify risks, foster collaboration among stakeholders, and regularly update sponsors to keep the trial on track.

What cities are hiring for Clinical Project jobs?

Cities with the most Clinical Project job openings:

What are the most commonly searched types of Clinical Project jobs?

The most popular types of Clinical Project jobs are:

What states have the most Clinical Project jobs?

States with the most job openings for Clinical Project jobs include:

Clinical Project jobs near you
Infographic showing various Clinical Project job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Project Scientist

Integrated Resources INC

Raritan, NJ • On-site

Contractor

Re-posted 3 days ago

Key responsibilities

  • Coordinate and manage CVM Medical Affairs clinical studies, including protocol development, budget forecasting, and timeline management.

  • Facilitate data collection for regulatory obligations such as PSUR, PADER, and annual IND reports.

  • Support the development and implementation of departmental processes to ensure compliance with company and regulatory standards.

Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

RESPONSIBILITIES:

Clinical Project Scientist -  Cardiovascular Metabolism (CVM) Medical Affairs 

  • The Clinical Project Scientist (CPS) is a key interface role in the CVM Medical Affairs (CVM MA) organization responsible for collaborating with therapeutic area teams to act as a liaison between therapeutic strategy and the clinical and operational implementation of product programs and clinical studies. 
  • The CPS plays a crucial role in ensuring that strategic level plans are executed in a timely, compliant, and within budget fashion in alignment with CVM MA goals. 
  • In addition, the role is critical in supporting all CVM MA activities including contracting, HCC requirements, SOP and process development, regulatory obligations etc. Scope of responsibility includes: 

1. In concert with the Associate Director, Clinical Project Scientist, the contractor CPS will direct the overall coordination and management of CVM MA clinical studies including: working in a highly matrix organization, the contract CPS will play a key role in interfacing with our partners to contribute to concept and protocol development, drive accurate budget forecasting and communicate variances, provide project management across the study to drive metrics and alignment to timelines, facilitate critical path analyses and optimization/contingency planning, escalate issues as appropriate for timely resolution, provide updates to senior management as directed. 

2. Provide input on the development of departmental processes to insure compliance to company and regulatory standards and procedures. Identify gaps and need for new process development. Participate in the development of training material for process roll-out as needed. 

3. Facilitate coordination for management of data collection for PSUR, PADER, annual IND and other regulatory obligations for CVM MAF products. 


4. Partner with Project Manager to insure timely and compliant contracting and HCC activities.

Qualifications

Education and Experience:

BA/BS degree is required. 

Advanced degree (MS, MBA) is desired. 

Strong leadership and collaboration skills are required. 

A minimum of 5 years working experience in clinical trial management within the pharmaceutical industry is required. 

Experience in Medical Affairs clinical trial management is highly desirable. 

A strong knowledge of clinical trial methodologies and ICH/GCP guidelines required. 

Financial planning and management experience required. 

Experience in leading cross functional teams in matrix environment is required. 

Strong interpersonal skills and ability to interact effectively with internal partners in a matrix setting are required. 

Ability to work in a fast-paced, dynamic environment is required. 

Strong communication skills required. 

Results/Performance driven. 

Ability to think creatively, critically, and proactively with strong problem solving skills is required. 

Therapeutic Area experience is desired. 

Additional Information

 Sneha - 732 549 5307





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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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