Senior Clinical Operations Lead: Phase I–III Programs

Merida Biosciences; Cambridge (MA); On-site; USD 200,000 - 240,000; Full time

Job summary

A biotechnology company in Cambridge is seeking an experienced Associate Director, Clinical Operations to oversee clinical trials from start-up to close-out. This role requires 7+ years of experience in clinical operations and a Bachelor's degree in Health or Life Sciences. The Associate Director will lead the operational aspects of Phase I–III trials, manage vendor relationships, and ensure compliance with ICH-GCP guidelines. The salary range for this role is $200,000 to $240,000, complemented by a competitive benefits package.

Qualifications

• 7+ years of clinical operations experience in biotech, pharma, or CRO settings.
• Experience leading global clinical trials.
• Strong understanding of ICH-GCP guidelines.

Responsibilities

• Lead operational execution of Phase I–III clinical trials.
• Manage CROs and vendors.
• Ensure trials comply with regulations and standards.

Skills

Clinical trial management

CRO management

Regulatory compliance

Problem-solving

Leadership

Education

Bachelor’s degree in Health or Life Sciences

Advanced degree preferred

Job description

A biotechnology company in Cambridge is seeking an experienced Associate Director, Clinical Operations to oversee clinical trials from start-up to close-out. This role requires 7+ years of experience in clinical operations and a Bachelor's degree in Health or Life Sciences. The Associate Director will lead the operational aspects of Phase I–III trials, manage vendor relationships, and ensure compliance with ICH-GCP guidelines. The salary range for this role is $200,000 to $240,000, complemented by a competitive benefits package.