This is a Contract opportunity which requires 3 days onsite in Valencia, California.

The Clinical Research Coordinator supports the successful execution of clinical trials, ensuring adherence to regulations and sponsor guidelines by supporting the Clinical Research team with a variety of ad hoc tasks and scheduling.

No C2C

Key Responsibilities:

• Support role for the clinical team as they lead studies from initiation to completion, ensuring consistent protocol communication.
• Ensure regulatory compliance by coordinating documentation and reporting.
• Collaborate on developing study materials, including informed consent forms, clinical reports, and protocols.
• Coordinate device supply and tracking at investigational sites.
• Maintain standard operating procedures and ensure departmental compliance.

Essential Requirements:

• Undergraduate degree in life sciences or related field

Desirable Qualifications:

• Post-baccalaureate degree
• Training in site management for clinical trials
• Clinical trial coordination experience in a clinic setting
• Familiarity with regulatory guidelines (21 CFR, Canadian Medical Device Regulations, ISO 14155)
• Proficient in Meridiv & Veeva Vault or related tools

Core Competencies:

• Strong organizational, recordkeeping, and problem-solving skills
• Excellent oral and written communication
• Ability to multitask with minimal supervision
• Solution-focused mindset
• Open to continuous learning

This role requires 3 days onsite in Valencia California

This is a contract opportunity with a target hourly rate of $45-$50 per hour