Senior Clinical Research Associate – West Coast

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

📋 Description

• Conducts on-site or remote monitoring activities related to Pre-Study, Initiation, Interim, and Close-Out visits to ensure that the investigational site’s facilities and staff remain suitable for the study's execution.

• Identifies and confirms that investigators possess the necessary qualifications, resources, facilities, equipment, and personnel to carry out the clinical study throughout its duration.

• Provides training to the staff at the investigational site as needed.

• When applicable, assists with the preparation of regulatory and/or ethics committee submissions.

• Engages in mentoring and training of new personnel, as well as conducting co-monitoring visits to evaluate the performance of junior staff.

⛳️ Requirements

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

• Significant on-site monitoring experience in phase 2/3 trials, preferably with a background in complex trials in oncology or rare diseases.

• Proficiency in English at a full working level.

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

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

• Willingness to travel nationally.

🏝️ Benefits

• Opportunities for training and career development within the organization.

• A strong focus on both personal and professional growth.

• A friendly and supportive workplace atmosphere.

• The chance to collaborate with colleagues from around the globe, with English as the primary language of communication.