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 conduct of studies.

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

• Provide necessary training to investigational site personnel.

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

• Mentor and train new employees.

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

⛳️ Requirements

• Bachelor’s degree in Life Sciences or an equivalent combination of education, training, and experience.

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

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

• Proficient in English with full working capabilities.

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

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

• Willingness to travel nationally.

🏝️ Benefits

• Options for remote work.

• Engaging and collaborative team atmosphere.

• Opportunity to impact patient-centered pharmaceutical treatments.

• Opportunities for mentoring and training.

• A diverse and inclusive work environment.