Remote Source

    Clinical Project Manager

    Regional
    Full-Time
    Mid (3-6 yrs)
    Operations & Project Management
    Posted on March 31, 2026
    ABOUT THE JOB
    The Clinical Project Manager (Clinical PM) plays a key role in the successful conduct of a clinical trial from inception through implementation and completion. The Clinical PM provides overall coordination and strategic management of a clinical trial, in conjunction with the clinical team and other functional groups. The Clinical Project Manager serves as the primary contact with the sponsor, clinical team, and other functional groups, while effectively delegating, and overseeing team members.
    The Clinical Project Manager ensures that all study team members are appropriately trained on the study and maintain compliance with GCP, the protocol, other associated documents, scope of work, and other clinical objectives. The Clinical PM serves as an effective team leader who manages and motivates team members using positive and productive methods of communication. The Clinical Project Manager also supports team member mentorship, as needed.
    HERE IS WHAT YOU WILL DO:
  1. Lead all clinical study operations, providing strategic/tactical planning, organization, and direction of study project(s) including but not limited to the oversight of clinical project timelines, reports, budgets, monitoring, site and vendor management, clinical supplies, and data collection
  2. Facilitate and foster positive, productive, and timely communication between sponsor, study team, and other functional groups
  3. Manage and motivate study team while serving as a mentor; mentorship may include identifying skills of the clinical team members and assisting with further professional development
  4. Provide proper financial oversight of study budget, including out of scope tracking, in conjunction with the Client Manager (CM) and ProTrials Finance Department
  5. Collaborate with senior management to provide study updates/progress, resourcing needs, sponsor issues, and health status at regularly scheduled intervals
  6. Drive the development, maintenance, and distribution of project plans based on project-specific requirements, throughout the life of the study (i.e., monitoring plan, communication plan, project management plan, eTMF plan, other plans as applicable)
  7. Manage studies in compliance with GCP, relevant SOPs, regulatory requirements, and project-specific plans
  8. Assess resourcing needs to ensure the study has the appropriate resources for the duration of the project
  9. Actively manage and track study risks (with team and sponsor input for potential obstacles that would delay the project’s progress while appropriately escalating issues
  10. Assess training needs of team members on the therapeutic area, protocol, special procedures/skills, and implement the appropriate training plans
  11. Delegate study team responsibilities and ensure that team members have the necessary tools and resources to effectively perform their role
  12. Monitor and manage the project’s progress and develop timelines with input from relevant stakeholders and sponsor approval; re-assess critical path for study progress and adjust timelines as needed
  13. Oversee activities and deliverables of outside vendors, as requested; ensure communication occurs between outside vendors, the team, and sponsor
  14. HERE IS WHAT YOU BRING TO THE TABLE:
  15. RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training and previous CRA experience
  16. Outstanding interpersonal, oral, and written communication skills
  17. Proven effectiveness as a team leader
  18. Prior experience successfully managing multifaceted studies from inception through implementation and completion
  19. Outstanding organizational and time management skills
  20. Experience managing projects in a virtual environment
  21. Demonstrated ability to lead by example and to encourage team members to seek solutions independently
  22. Proficiency in Microsoft Word, Excel, and PowerPoint are required
  23. Experience with MS Project and OneNote a plus
  24. HERE IS WHAT WE OFFER:
  25. Your wellness matters to us – that’s why we provide full medical, dental, and vision insurance options for you and your family.
  26. We know life doesn’t pause for work – we provide flexible PTO so you can take care of what matters, both personally and professionally.
  27. You invest in your future – and so do we. Our 401(k) plan includes a company match to help you reach your financial goals.
  28. At ProTrials, we are committed to your growth. Whether you’re looking to expand your skills or take the next step in your career, we provide the support and opportunities you need to keep moving forward.
  29. We have the best coworkers, if we do say so ourselves.
  30. Apply for this position
    Provides clinical research services to pharmaceutical, biotechnology and medical device companies.
    51-200 employees
    Healthcare & Life Sciences
    HQ: United States