Clinical Research Coordinator (CRC)
Hiring Now | 2 Open Positions
Work Hours: 9:00 AM – 5:00 PM
Salary: Competitive
Languages Required: Hindi, English
Experience: Freshers & Experienced Candidates Welcome
Location: Hospital / Clinical Trial Site
Gender: Male / Female
Role: Clinical Research Coordinator / CRC Trainee
Eligibility
Degree holders from the following streams may apply:
B. Pharma, M. Pharma, B. Tech (Bio/Med), MSc (Life Sciences), BSc, BAMS, BUMS, or related health/biomedical fields.
Job Description
The Clinical Research Coordinator (CRC) will support day-to-day site operations for clinical trials, ensuring compliance with regulatory guidelines and Good Clinical Practice (GCP). This role requires strong coordination, communication, and documentation skills.
Key Responsibilities
Understanding of clinical research regulations, ICH-GCP guidelines, and site SOPs.
Act as a communication bridge among physicians, patients, monitors, and site leadership.
Support Senior CRC in:
Screening & informed consent process
Randomization and enrollment
Patient follow-up (including telephonic follow-up)
Maintain the Investigator Site File (ISF) and source documents as per Good Documentation Practices.
Participate in:
Site Initiation Visits (SIV)
Monitoring Visits (MV)
Site Close-Out Visits (SCV)
Perform CRF / e-CRF data entry and resolve data queries.
Coordinate with local or central laboratories and logistics teams for biological sample shipment.
Assist in drug accountability, temperature logs, and pharmacy coordination.
Support scheduling of study procedures, visit planning, and study material management.
Prepare file notes, weekly reports, and monthly activity reports for the reporting authority.
Track study progress, patient status, screening log, enrolment status, and overall study activities.
How to Apply
UPLOAD YOUR CV
(Freshers with strong interest in Clinical Research are encouraged to apply.)
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