Clinical Research Coordinator
Location: Boston, MA (Hybrid)
Employment Type: Contract (W2 Only)
Experience: 0–3 Years
Job Summary
Seeking a Clinical Research Coordinator to support clinical trials, patient enrollment, study documentation, and regulatory compliance while ensuring adherence to GCP guidelines.
Key Responsibilities
- Coordinate clinical study activities
- Maintain Trial Master File (TMF) documentation
- Schedule patient visits and study procedures
- Assist with informed consent documentation
- Support regulatory submissions and audit readiness
- Collaborate with investigators and study sponsors
Qualifications
- Bachelor's degree in Life Sciences, Biology, Pharmacy, Nursing, or related field
- Basic knowledge of GCP and FDA regulations
- Strong communication and documentation skills
E: Pavan@unitedconsultinghub.com
