Senior Clinical Studies Lead — Study Ops & Compliance

RadNet; Somerville (MA); Hybrid; USD 71,000 - 96,000; Full time

Job summary

RadNet is seeking a Senior Clinical Studies Associate in Somerville, Massachusetts, to support the planning and execution of clinical studies. This role involves developing study documentation, ensuring regulatory compliance, and managing project timelines effectively.

The ideal candidate has a Bachelor’s degree in life sciences, at least 2 years of clinical research experience, and strong organizational skills. The position allows for remote, hybrid, or office work.

Qualifications

• Bachelor’s degree in life sciences or related field required.
• Minimum 2 years of related clinical research experience needed.
• Working knowledge of Good Clinical Practice (GCP) and applicable regulatory guidelines is essential.

Responsibilities

• Support the planning, execution, and management of clinical studies.
• Draft and maintain clinical study documentation in compliance with guidelines.
• Prepare and coordinate IRB submissions and related activities.

Skills

Attention to detail

Organizational skills

Communication skills

Collaboration skills

Education

Bachelor’s degree in life sciences or related field

Advanced degree preferred

Tools

Clinical trial management systems

Job description

RadNet is seeking a Senior Clinical Studies Associate in Somerville, Massachusetts, to support the planning and execution of clinical studies. This role involves developing study documentation, ensuring regulatory compliance, and managing project timelines effectively.

The ideal candidate has a Bachelor’s degree in life sciences, at least 2 years of clinical research experience, and strong organizational skills. The position allows for remote, hybrid, or office work.