Senior Clinical Trial Manager

GQR; United States; Remote; USD 150,000 - 165,000; Full time

Job summary

A global biopharmaceutical company is seeking a Senior Clinical Trial Manager to oversee clinical trial operations, focusing on vendor and site management. This full-time contractor role will involve leading study initiatives while ensuring compliance with regulatory guidelines and maintaining high standards in study management.

Benefits

Medical insurance

Vision insurance

401(k)

Paid maternity leave

Paid paternity leave

Disability insurance

Qualifications

• 8+ years in Pharma/Biotech with global trial experience.
• Strong leadership in sponsor-side trial management.
• Proficiency in managing post-marketing or observational studies is a plus.

Responsibilities

• Manage all aspects of assigned study operations including vendors and site oversight.
• Lead the development of study-related documents such as informed consent forms.
• Monitor and maintain the Trial Master File to ensure document completeness.

Skills

Leadership

Risk Mitigation

Education

Bachelor’s degree in science or healthcare-related discipline

Job description

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Job Title:

Senior Clinical Trial Manager (Contractor)

Location:

Remote – US Only (NO C2C)

Summary:

Our client, a global biopharmaceutical company, is seeking a Senior Clinical Trial Manager (CTM) to act as the Lead Study Manager on a key study initiative. This is a full-time contract opportunity focused on overseeing end-to-end clinical trial operations including vendor and site management, risk mitigation, and essential documentation control. The role is remote, based in Massachusetts.

Key Responsibilities:

• Manage all aspects of assigned study operations including vendors, supply logistics, and site oversight.
• Lead the development and review of study-related documents such as informed consent forms and risk plans.
• Actively contribute to and lead study team meetings.
• Monitor and maintain the Trial Master File and ensure document completeness.
• Assist with clinical budgeting and financial tracking.
• Identify risks and implement strategic solutions.
• Ensure studies adhere to SOPs and regulatory guidelines.

Qualifications:

• Bachelor’s degree in science or healthcare-related discipline.
• 8+ years in Pharma/Biotech, with global trial experience.
• Strong leadership in sponsor-side trial management.
• Proficiency in managing post-marketing or observational studies is a plus.
• Availability for up to 10% travel.

Pay Rate:

$75.00/hr (40 hours per week; overtime after 40 hours)

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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Inferred from the description for this job

Medical insurance

Vision insurance

Paid paternity leave

401(k)

Disability insurance

Paid maternity leave

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