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Clinical Research Coordinator (Crc)

Micro Data Labs
0-1 years
Not Disclosed
amritsar, Hyderabad, kanpur, India
4 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Clinical Research Coordinator (CRC)

Company: Micro Data Labs (MDL)
Position: Clinical Research Coordinator (CRC)
Employment Type: Full-Time

Available Locations

  • Kanpur – 1 Position

  • Hyderabad – 1 Position

  • Amritsar – 1 Position

  • Ludhiana – 1 Position

Note: Candidates who can join immediately and reside near the respective job location will be given preference.


Job Summary

Micro Data Labs (MDL) is seeking dynamic, proactive, and detail-oriented Clinical Research Coordinators (CRCs) to support the successful execution of clinical research studies. The ideal candidate should possess strong communication, organizational, and documentation skills while ensuring compliance with study protocols, GCP guidelines, and regulatory requirements.

Freshers with relevant educational backgrounds are encouraged to apply.


Key Responsibilities

Clinical Trial Coordination

  • Support the day-to-day operational activities of clinical trials.

  • Coordinate study-related activities with investigators, sponsors, and site staff.

  • Ensure smooth execution of clinical research studies according to approved protocols.

Data Collection and Management

  • Collect, record, verify, and update clinical trial data accurately and in a timely manner.

  • Maintain study records and ensure data integrity throughout the study lifecycle.

  • Prepare and share weekly study progress reports and data collection updates with clients and stakeholders.

Query Management

  • Review and respond to data queries.

  • Ensure timely resolution of discrepancies and missing information.

  • Coordinate with relevant stakeholders to maintain data quality standards.

Patient Coordination

  • Conduct patient follow-ups to ensure protocol compliance and visit adherence.

  • Maintain regular communication with study participants.

  • Support patient retention and engagement throughout the study duration.

Compliance and Documentation

  • Maintain accurate study documentation and regulatory files.

  • Ensure compliance with GCP guidelines, study protocols, and applicable regulations.

  • Support monitoring visits, audits, inspections, and sponsor reviews.

Stakeholder Communication

  • Coordinate effectively with investigators, site teams, sponsors, CROs, and other study stakeholders.

  • Facilitate communication between study teams and external partners when required.


Qualifications

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Nursing

    • Biotechnology

    • Related Healthcare or Science Discipline


Experience

  • Prior experience as a Clinical Research Coordinator is preferred.

  • Freshers with relevant qualifications may also apply.