Job Summary
The Clinical Research Coordinator is responsible for managing and overseeing clinical trials in compliance with regulatory guidelines, study protocols, and ethical standards. They act as a link between investigators, participants, sponsors, and regulatory bodies to ensure smooth execution of clinical research studies.
Key Responsibilities
- Coordinate and manage day-to-day clinical trial activities
- Ensure studies are conducted according to protocol, GCP (Good Clinical Practice), and regulatory requirements
- Recruit, screen, and enroll study participants
- Obtain informed consent from participants
- Schedule and conduct study visits
- Collect, record, and maintain accurate clinical data
- Manage Case Report Forms (CRFs) and electronic data capture systems
- Monitor patient safety and report adverse events (AEs/SAEs)
- Maintain study documentation including Investigator Site Files (ISF)
- Coordinate with sponsors, CROs, and ethics committees
- Assist in site audits and inspections
- Ensure proper storage and handling of investigational products
Required Qualifications
- Bachelor’s degree in:
- Life Sciences
- Pharmacy
- Nursing
- Biotechnology or related field
- Certification in clinical research (preferred but not mandatory)
Experience
- 0–2 years (for entry-level CRC)
- 2–5 years (for experienced CRC roles)
- Prior experience in clinical trials or hospital research settings is preferred
Key Skills
- Knowledge of ICH-GCP guidelines
- Strong organizational and documentation skills
- Attention to detail
- Good communication and interpersonal skills
- Ability to manage multiple studies simultaneously
- Familiarity with clinical trial software (e.g., EDC systems)
Work Environment
- Hospitals
- Clinical research organizations (CROs)
- Pharmaceutical companies
- Academic research institutions
Pay: $33.01 - $39.76 per hour
Benefits:
- Dental insurance
- Employee assistance program
- Flexible schedule
- Parental leave
- Retirement plan
- Tuition reimbursement
Work Location: In person