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Clinical Project Manager - ONSITE

Plymouth, Minnesota

Piper Companies Logo

Job Id:
156694

Job Category:

Job Location:
Plymouth, Minnesota

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Piper Clinical Solutions

Position Owner:
Anne Green

Piper Companies is seeking a Clinical Project Manager to oversee the planning and execution of clinical studies within the healthcare and medical device industry. The Clinical Project Manager role is ideal for a professional with experience in clinical trial management, regulatory compliance, and cross-functional coordination. The Clinical Project Manager will need to sit on site several days per week in Plymouth, MN and is a long term contract.


Responsibilities of the Clinical Project Manager:

  • Manage one or more clinical projects, ensuring timelines, budgets, and deliverables are met.
  • Coordinate with R&D, Regulatory Affairs, and other departments to develop study plans and trial strategies.
  • Oversee site selection, vendor management, and regulatory submissions.
  • Monitor compliance with protocols and regulatory standards, addressing deviations as needed.
  • Provide training to internal teams and site personnel, and lead key meetings with investigators and stakeholders.
  • Support process improvement initiatives and mentor junior project managers.

Requirements of the Clinical Project Manager:

  • Bachelor’s degree in health sciences or related field.
  • Minimum 2 years of clinical project management experience (cardiovascular experience preferred).
  • Strong knowledge of ISO standards and local clinical trial regulations.
  • Proven ability to manage budgets, timelines, and cross-functional teams.
  • Fluent in English, computer literate, and committed to high ethical standards.
  • Ability to work in Plymouth, MN

Compensation for the Clinical Project Manager includes:

  • $50.00 - $70.00 per hour
  • Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave Required by Law


Keywords:

Clinical Project Manager, clinical trials, project management, regulatory compliance, ISO standards, cardiovascular studies, vendor management, site selection, protocol design, data management, monitoring plan, cross-functional collaboration, Plymouth MN, healthcare industry, medical device, budgeting, resource management.


This job opens for applications on 12/19/2025. Applications for this job will be accepted for at least 30 days from the posting date.


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