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Clinical Research Coordinator (Crc)

Fresher years
3-5 LPA
2 Nov. 26, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.)