Senior Clinical Research Associate – West Coast

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

📋 Description

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

• Ensure that investigational facilities and personnel are suitable for the execution of the study.

• Identify and verify the qualifications, resources, facilities, equipment, and personnel of investigators.

• Provide training to investigational site staff as required.

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

• Mentor and train new team members.

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

⛳️ Requirements

• A degree from a College or University in Life Sciences or a comparable mix of education, training, and experience.

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

• Ideally, familiarity with complex trials in oncology or rare diseases.

• Full working proficiency in English.

• Competence in planning, multitasking, and working effectively in a dynamic team setting.

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

• Willingness to travel nationally.

🏝️ Benefits

• Option for remote work.

• A passionate and collaborative team atmosphere.

• Opportunity to contribute to the delivery of safe and effective pharmaceutical treatments to patients.

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