Clinical Project Manager

Thor Companies; Minnesota; On-site; USD 140,000 - 160,000; Full time

Job summary

A leading company is seeking a Clinical Project Manager to oversee two ongoing clinical trials within a fast-paced startup environment. The ideal candidate will have extensive experience in the life sciences sector and be proactive in managing clinical trial operations, ensuring compliance, and driving project timelines. A competitive salary and comprehensive benefits package are on offer.

Qualifications

• 7–10 years of experience in the life sciences industry.
• 3–5 years of direct experience managing clinical trials independently.
• Prior experience in medical devices strongly preferred.

Responsibilities

• Lead day-to-day operations for two concurrent clinical trials.
• Oversee clinical trial execution in collaboration with internal stakeholders and external partners.
• Manage relationships with CROs and ensure compliance with regulatory standards.

Skills

Proactivity

Detail-oriented

Adaptability

Job description

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This range is provided by Thor Companies. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$140,000.00/yr - $160,000.00/yr

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About the Company

Our client is a well-funded, fast-growing medical device startup developing innovative solutions in the hypertension space. Backed by strong investment and led by a lean, high-performing team, the company is entering a key phase of clinical development with strong growth on the horizon.

The Opportunity

They are seeking a Clinical Project Manager to take ownership of two ongoing clinical trials. This is a high-impact, hands-on role with strong visibility across the organization. The ideal candidate is detail-oriented, proactive, and thrives in a fast-paced, startup environment.

Key Responsibilities

• Lead day-to-day operations for two concurrent clinical trials
• Oversee clinical trial execution in collaboration with internal stakeholders and external partners
• Manage relationships with CROs and ensure compliance with regulatory and protocol standards
• Drive timelines, budgets, and deliverables across both studies
• Serve as the primary point of contact between internal teams, CROs, and regulatory stakeholders

Qualifications

• 7–10 years of experience in the life sciences industry (biotech, pharma, or medical devices)
• 3–5 years of direct experience managing clinical trials independently
• Prior experience in medical devices strongly preferred
• Proven ability to manage CROs and vendors
• High-energy, adaptable, and comfortable taking initiative in a startup or lean team setting

Offering a salary between $140,000 and $160,000, depending on experience, along with a comprehensive benefits package.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing

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