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Temporary Contract Clinical Project Manager Jobs

Bioclinica

Clinical Project Manager

Princeton, NJ · On-site

... Clinical Project Manager will focus on study start up through close out activities and perform ... Possessing a thorough understanding of the project contract and totals needed for monthly revenue ...

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Clinical Project Manager III

Bedford, MA · On-site

Provides project planning and tracking to clinical project team members and the Program Manager and/pr Clinical Research Manager. Drive the integration of activities between functions.

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Clinical Project Manager III

Bedford, MA · On-site

Provides project planning and tracking to clinical project team members and the Program Manager and/pr Clinical Research Manager. Drive the integration of activities between functions.

ClinChoice

Senior Clinical Project Manager

OR · On-site +1

We are currently recruiting for a Senior Clinical Project Manager to support projects across ... Contract Research Organization #LI-VH1 #LI-Senior #LI-FULLTIME

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Clinical Project Manager III

Bedford, MA · On-site

Provides project planning and tracking to clinical project team members and the Program Manager and/pr Clinical Research Manager. Drive the integration of activities between functions.

AC Wellness

Clinical Project Manager

Cupertino, CA · On-site

The Clinical Project Manager leads and coordinates cross-functional clinical and operational initiatives that support the strategic goals of AC Wellness. This role is responsible for defining project ...

AC Wellness

Clinical Project Manager

Cupertino, CA · On-site

The Clinical Project Manager leads and coordinates cross-functional clinical and operational initiatives that support the strategic goals of AC Wellness. This role is responsible for defining project ...

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How much do temporary contract clinical project manager jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for temporary contract clinical project manager 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 does a Temporary Contract Clinical Project Manager do?

A Temporary Contract Clinical Project Manager is responsible for overseeing and managing clinical trials or research projects for a specific period, usually to fill a short-term need or support a particular study. They coordinate project timelines, budgets, and teams to ensure clinical studies are conducted according to regulatory standards and company protocols. Their duties often include managing communication between stakeholders, ensuring compliance, and solving any issues that arise during the course of the project. This role is typically filled by professionals with strong project management experience and a background in clinical research.

What are the key skills and qualifications needed to thrive as a Temporary Contract Clinical Project Manager, and why are they important?

To thrive as a Temporary Contract Clinical Project Manager, you need a background in life sciences or related fields, experience managing clinical trials, and knowledge of regulatory requirements. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and project management software is typically required, along with certifications such as PMP or equivalent being advantageous. Strong organizational, leadership, and communication skills help in coordinating teams, managing timelines, and ensuring compliance. These skills are vital to deliver clinical projects successfully, maintain regulatory standards, and meet tight contract deadlines.

What are some unique challenges faced by Temporary Contract Clinical Project Managers, and how can they be addressed?

Temporary Contract Clinical Project Managers often need to quickly adapt to new organizational cultures and project workflows, as they are brought in for specific studies or timelines. One challenge is establishing trust and clear communication with existing teams in a short timeframe. To address this, it's helpful to proactively engage stakeholders, clarify project goals early, and leverage strong organizational skills to stay on track with deliverables. Being adaptable and demonstrating expertise can help contract managers integrate smoothly and drive project success.

What is the difference between Temporary Contract Clinical Project Manager vs Clinical Research Associate?

AspectTemporary Contract Clinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, project management certification is a plusRequires a Bachelor's degree in life sciences or related field; often includes GCP or ICH training
Work EnvironmentManages multiple projects, oversees teams, and liaises with sponsorsMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsageUsed by pharmaceutical companies, CROs, biotech firms for project oversightCommonly employed by CROs, pharmaceutical companies for trial monitoring

The main difference is that the Temporary Contract Clinical Project Manager oversees entire clinical projects and manages teams, while the Clinical Research Associate focuses on monitoring clinical trial sites and ensuring compliance. Both roles require similar educational backgrounds and certifications but differ in scope and responsibilities.

More about Temporary Contract Clinical Project Manager jobs
What cities are hiring for Temporary Contract Clinical Project Manager jobs? Cities with the most Temporary Contract Clinical Project Manager job openings:
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Temporary Contract Clinical Project Manager jobs near you
Infographic showing various Temporary Contract Clinical Project Manager job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 70% Full Time, 16% Part Time, 1% Temporary, and 12% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.
Clinical Project Manager

Clinical Project Manager

Bioclinica

Princeton, NJ • On-site

Full-time

Posted 16 days ago

Job description

Company Description
Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials. We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia. We are headquartered in Doylestown, PA. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device organizations
Job Description
The Clinical Project Manager will focus on study start up through close out activities and perform project analysis while highlighting leadership skills in therapeutic areas such as Neuroscience, Musculoskeletal, Oncology, Cardiovascular, and more. This individual would be driven, dedicated and adaptable in a fast-paced environment. Project Management experience within a CRO is highly desirable.
Primary Responsibilities
Identifies project guidelines and communication needs by:
  • Reviewing study requirements and response assessment criteria and collaborates with key stakeholders to develop study start-up activities and associated documents
  • Defining project plans (i.e. timelines, milestones and limitations for project staff)
  • Establishing project reporting schedules
  • Providing project updates to BD Director, Global Services Managing Directors, Sponsor representative(s) on schedule
  • Communicating timely, appropriate project information to project teams, sites and company/sponsor representative(s)

Performs project analysis and management by:
  • Identifying critical project success factors for tracking, analysis and reporting
  • Determining needed resources for project completion and communicating needs to appropriate departmental managers
  • Collaborating with department leaders for appropriate training of those involved with the project toward excellence in successful and timely completion of project
  • Performing financial tasks including monthly billing, forecasting, project scope reviews and amendments, and pass-through cost management
  • Possessing a thorough understanding of the project contract and totals needed for monthly revenue reporting
  • Understanding SOPs and working closely with QA for clarification and documentation of deviations
  • Training and maintaining project team knowledge and applications of SOPs
  • Communicating all protocol clarifications/revisions to project team
  • Coordinating site management of data collection with internal and external teams

Provides project team leadership by:
  • Leading by example with professional and collaborative conduct
  • Developing and delivering team project training
  • Establishing team performance expectations and guidelines
  • Providing input to departmental managers of respective team members' performance level
  • Analyzing team performance for consistency/quality within established project guidelines
  • Collaborating with the departmental managers for team coaching/mentoring

Supports Business Development efforts by:
  • Collaborating with BD Director in the development and presentation of company capabilities calls/meetings
  • Attending professional meeting(s) as Company representative
  • Delivering polished Investigator Meeting presentation projecting solid comprehension of project/protocol and company services

Oversees project close out by:
  • Assisting with coordination of submission activities, as applicable
  • Assisting with initiating and overseeing all project close out activities to completion

Performs supervisory functions by, if applicable:
  • Communicating job expectations
  • Planning, monitoring and appraising job results
  • Coaching, counseling and disciplining staff
  • Initiating, coordinating and enforcing systems, policies and procedures
  • Approving direct reports time sheets, requests for time off and/or overtime
  • Performing timely performance evaluations of direct reports
  • Coordinating and conducting new hire interviews; facilitating hiring decision
  • Training new hires on departmental processes and responsibilities

Maintains Quality Service and Departmental Standards by:
  • Reading, understanding and adhering to organizational Standard Operating Procedures ("SOP")
  • Establishing and enforcing departmental standards
  • Reviewing and updating company SOPs related

Secondary Responsibilities
Contributes to team effort by:
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to accomplish results
  • Performing other duties as assigned and deemed necessary

Maintains Technical Knowledge by:
  • Attending and participating in applicable company sponsored training

Qualifications
Education:
  • Bachelor's degree required or commensurate experience level. Educational majors in life sciences, pharmacy, nursing, or other healthcare field highly desirable

Experience:
  • Previous management or project experience in clinical development of investigational medications required
  • 1-3 years clinical trials experience within a CRO or pharmaceutical research organization required; preferably in a project management related role.
  • Working knowledge of GCH, ICH guidelines and FDA regulations
  • Medical Imaging experience a plus
  • Experience working with computer software including Word, Excel, Access and Project preferred

Additional skill set:
  • Strong interpersonal and communication skills, both verbal and written
  • Strong organizational and leadership skills
  • Goal oriented
  • Ability to maintain professional and positive attitude

Additional Information
Working conditions:
  • Travel: 0-20%
  • Lifting: 0-15lbs
  • Other: Computer work for long periods of time

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

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