Senior Clinical Research Associate – West Coast

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

📋 Description

• Conduct Pre-Study, Initiation, Interim, and Close-Out monitoring visits either on-site or remotely.

• Ensure that investigational facilities and personnel are sufficiently equipped for the study's execution.

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

• Provide training to site staff as necessary.

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

• Mentor and train new team members.

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

⛳️ Requirements

• Bachelor's degree in Life Sciences or a comparable combination of education, training, and experience.

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

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

• Full working proficiency in English.

• Capable of planning, multitasking, and thriving in a dynamic team environment.

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

• Willingness to travel nationally.

🏝️ Benefits

• Options for remote work.

• A collaborative team atmosphere.

• Opportunities for mentoring and training.

• The chance to contribute to pharmaceutical treatments that benefit patients globally.