What are the responsibilities and job description for the Clinical Research Coordinator - Contract position at Blue Bridge People?
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.
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)
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
Salary : $45 - $50