About This Role
Coordinating and supporting all aspects of clinical trials and research studies is the core of this role, including subject recruitment, data collection, regulatory compliance, and specimen handling. The position suits a highly organized and motivated individual to join a research team.
Responsibilities
- Coordinate day-to-day clinical research activities to ensure study protocols are followed
- Recruit, screen, and enroll study participants
- Obtain informed consent and ensure ethical conduct in all study interactions
- Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples)
- Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs)
- Maintain accurate and timely documentation in case report forms and electronic databases
- Communicate with sponsors, monitors, and IRBs regarding study progress and compliance
- Schedule participant visits and follow-ups; ensure visit windows are met
- Ensure proper storage, handling, and accountability of investigational products, if applicable
- Maintain regulatory documents and assist with IRB submissions
Requirements
- Bachelor's degree in a health-related field required
- At least 1–2 years of experience in clinical research preferred
- Phlebotomy certification or MA certification preferred
- Knowledge of Good Clinical Practice (GCP) and regulatory guidelines
- Excellent organizational skills and attention to detail
- Strong interpersonal and communication skills
- Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms)
- Ability to work independently and as part of a multidisciplinary team
Nice to have:
- Experience working in clinical trials, especially in a hospital or academic setting
- Familiarity with IRB processes and clinical trial documentation
- Bilingual skills (depending on patient population) may be a plus
Important Details
- Schedule: 8 hour shift, Monday to Friday, weekends as needed
About the Company
We are seeking a Clinical Research Coordinator (CRC) to join our research team.
