Senior Clinical Research Associate

This is a fully remote position, open to applicants in Massachusetts.

📋 Description

• Conduct on-site or remote monitoring visits during Pre-Study, Initiation, Interim, and Close-Out phases.

• Ensure that investigational facilities and personnel remain suitable throughout the duration of the study.

• Identify investigators and confirm their qualifications, resources, facilities, equipment, and staff adequacy.

• Provide training to investigational site staff as required.

• Assist in the preparation of regulatory and/or Ethics Committee submissions when necessary.

• Guide and mentor new staff members.

• Carry out co-monitoring visits to evaluate the performance of junior staff.

⛳️ Requirements

• A college or university degree in Life Sciences or a comparable combination of education, training, and experience.

• Significant on-site monitoring experience in Phase 2/3 clinical trials.

• Preferably, experience with complex trials in oncology or rare diseases.

• Full working proficiency in English is required.

• Capability to plan, manage multiple tasks, and operate within a dynamic team environment.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel nationally.

🏝️ Benefits

• Options for remote work.

• A collaborative and passionate team environment.

• Opportunities to significantly impact patients' lives.

• A diverse and inclusive workplace where every voice is valued.