Clinical Project Manager - ONSITE

Piper Companies; Plymouth; On-site; GBP 60,000 - 80,000; Full time

Job summary

A healthcare and medical device firm is seeking a Clinical Project Manager to oversee the planning and execution of clinical studies. The ideal candidate will have at least 2 years of clinical project management experience, preferably in cardiovascular studies. Responsibilities include managing project timelines and budgets, ensuring compliance with ISO standards and local regulations. This long-term contract position requires on-site presence several days a week in Plymouth, MN. Competitive hourly compensation is offered, along with comprehensive benefits.

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.
• Proficient in managing timelines and deliverables.
• Strong knowledge of local clinical trial regulations.

Responsibilities

• Manage one or more clinical projects, ensuring timelines, budgets, and deliverables are met.
• Coordinate with R&D, Regulatory Affairs, and other departments.
• Monitor compliance with protocols and regulatory standards.

Skills

Clinical trial management

Regulatory compliance

Cross-functional coordination

Budget management

ISO standards knowledge

Fluent in English

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

• 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

• 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

• $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.