Clinical Project Manager

-; Plymouth; On-site; GBP 93,000 - 109,000; Full time

Job summary

A leading organization in the medical device industry is seeking a Clinical Project Manager for a 12-month contract onsite in Plymouth. Responsibilities include managing clinical study timelines, budgets, and regulatory compliance with an emphasis on cardiovascular medical devices. Key qualifications include a Bachelor's degree and at least 2 years of related experience. Competitive salary of $125,000‑$145,000 per year with comprehensive benefits is offered.

Benefits

Medical insurance

Dental insurance

Vision insurance

401K

Qualifications

• 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.

Responsibilities

• Manage clinical study timelines and budgets, including vendor selection.
• Facilitate communication among cross‑functional teams and investigational sites.
• Oversee regulatory submissions and ensure compliance with ISO and local regulations.

Skills

Clinical project management

Communication skills

Organizational skills

Knowledge of ISO standards

Proficiency in project management tools

Education

Bachelor’s degree in health sciences or related field

Tools

Microsoft Office Suite

Job description

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.