Clinical Project Manager - ONSITE

-; Plymouth; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A healthcare firm is seeking a Clinical Project Manager to lead the planning and execution of clinical studies. This role requires experience in clinical trial management, regulatory compliance, and project coordination. The ideal candidate should possess a Bachelor's degree and a minimum of 2 years of relevant experience. The position is hybrid and includes competitive compensation with comprehensive benefits. The role demands onsite presence in Plymouth several days a week.

Benefits

Health insurance

Vision insurance

Dental insurance

PTO

Paid Holiday and Sick Leave

Qualifications

• Minimum 2 years of clinical project management experience, preferably in cardiovascular studies.
• Strong knowledge of ISO standards and local clinical trial regulations.
• Ability to train internal teams and site personnel.

Responsibilities

• Manage one or more clinical projects, ensuring timelines and budgets are met.
• Coordinate with departments to develop study plans and trial strategies.
• Monitor compliance with protocols and regulatory standards.

Skills

Clinical trial management

Regulatory compliance

Cross-functional coordination

Project management

Budget management

Education

Bachelor's degree in health sciences or related field

Job description

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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