Job Title: Clinical Research Coordinator
Location: Beverly Hills, CA
job type: Contrat (Part-time)
Job Summary:
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the day-to-day operations of clinical research studies. This role involves ensuring that clinical trials are conducted in compliance with study protocols, regulatory requirements, and ethical standards. The CRC will collaborate with principal investigators, healthcare providers, and study participants to facilitate the smooth execution of trials, from participant recruitment through data collection and reporting.
Key Responsibilities:
- Coordinate Clinical Trials: Manage and oversee all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up.
- Study Compliance: Ensure adherence to study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements (IRB, FDA, etc.).
- Data Management: Collect, document, and maintain accurate clinical data, ensuring confidentiality and integrity for audits and monitoring purposes.
- Participant Monitoring: Monitor participants for adverse events and other study-related health concerns, reporting findings promptly to investigators and regulatory bodies.
- Study Documentation: Maintain detailed study records, including informed consent forms, case report forms, and regulatory submissions.
- Communication: Act as the liaison between study sponsors, investigators, regulatory authorities, and other stakeholders to ensure smooth trial progress.
- Regulatory Submissions: Prepare and submit study-related documents for Institutional Review Board (IRB) approval and ensure timely reporting of study progress.
Qualifications:
- Bachelor’s degree in healthcare, life sciences, or a related field (Master’s degree preferred).
- At least 1-2 years of experience in clinical research or a similar role.
- Knowledge of GCP guidelines, clinical trial regulations, and ethical standards in research.
- Strong organizational, communication, and interpersonal skills.
- Ability to work independently and as part of a multidisciplinary team.
Preferred Skills:
- Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP).
- Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) tools.