Clinical Trial Manager

Stratacuity: Proven Scientific Placement; Boston; Hybrid; USD 90,000 - 120,000; Full time

Job summary

A leading clinical trial organization is seeking a Clinical Trials Manager to oversee planning and execution of Phase 1-3 studies. Responsibilities include managing timelines, budgets, and vendors. Ideal candidates have 4-6 years of clinical operations experience and knowledge of ICH-GCP. This position is hybrid based in Bedford, MA, offering a collaborative work environment and career growth opportunities.

Qualifications

• 4-6 years in clinical operations (biotech, pharma, or CRO).
• Experience managing multiple clinical trials and site visits.
• Strong knowledge of ICH-GCP and drug development.

Responsibilities

• Oversee study timelines, budgets, and vendor performance.
• Lead site and vendor qualification and selection.
• Support data review and database lock activities.

Skills

Clinical operations experience

Knowledge of ICH-GCP

Microsoft Office proficiency

Excellent communication skills

Problem-solving skills

Education

Bachelor’s degree in scientific or healthcare field

Tools

MS Project

Job description

Location: Bedford, MA (Hybrid)

Therapeutic Area: Rare Disease

Job Overview: As a Clinical Trials Manager, you’ll lead the planning and execution of Phase 1–3 clinical studies and open-label extensions. You’ll manage CROs, vendors, and clinical sites to ensure trials are delivered on time, within budget, and in full compliance with GCP and regulatory standards.

Primary Job Responsibilities:

• Oversee study timelines, budgets, and vendor performance
• Lead site and vendor qualification and selection
• Contribute to protocol, ICF, and study document development
• Coordinate drug supply forecasting and delivery
• Support data review and database lock activities
• Identify and mitigate study risks
• Ensure audit readiness and documentation compliance
• Collaborate cross-functionally to meet Clinical Development Plan goals

Primary Job Requirements:

• 4–6 years in clinical operations (biotech, pharma, or CRO)
• Experience managing multiple clinical trials and site visits
• Strong knowledge of ICH-GCP and drug development
• Bachelor’s degree in a scientific or healthcare field preferred
• Rare disease and neurology experience a plus
• Proficient in Microsoft Office and MS Project
• Excellent communication, organization, and problem-solving skills

About Stratacuity:

Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

PROVEN SCIENTIFIC PLACEMENT

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