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Clinical Project Manager

Plymouth, Minnesota

Piper Companies Logo

Job Id:
157015

Job Category:

Job Location:
Plymouth, Minnesota

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Piper Clinical Solutions

Position Owner:
Madalyn Barry

Piper Companies is seeking a Clinical Project Manager to join a leading organization in the medical device industry for a 12-month contract position based onsite in Plymouth, MN (4 days per week). The Clinical Project Manager will oversee clinical study execution, manage budgets, and ensure compliance with regulatory standards, with a strong preference for experience in cardiovascular medical devices.

 

Responsibilities of the Clinical Project Manager include:

  • Manage clinical study timelines and budgets, including vendor selection and contract oversight.
  • Facilitate communication among cross-functional teams (R&D, Regulatory, Marketing) and investigational sites.
  • Oversee regulatory submissions and ensure compliance with ISO and local regulations.
  • Provide input on protocol design, case report forms, and monitoring plans.
  • Coordinate investigator meetings, steering committees, and study-specific training for internal and site personnel.

 

Qualifications for the Clinical Project Manager include:

  • Minimum of a Bachelor’s degree in health sciences or related field.
  • At least 2 years of clinical project management experience; cardiovascular or cardiology device experience strongly preferred.
  • Proven ability to manage study budgets and timelines effectively.
  • Strong knowledge of ISO standards and clinical trial regulations.
  • Excellent communication, organizational, and leadership skills; proficiency in project management tools and Microsoft Office Suite.

 

Compensation for the Clinical Project Manager: ·

  • Salary: $125,000-$145,000/year (USD)
  • Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K.

 

This job opens for applications on 12/17/25. Applications for this job will be accepted for at least 30 days from the posting date.

 

Keywords: clinical project management, clinical trials, medical device, cardiology, GCP, ISO compliance, regulatory submissions, budgeting, vendor management, protocol design, cross-functional collaboration, project timelines, investigator meetings, clinical operations.

 

#LI-MB1 #LI-ONSITE

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