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    • Skills: Basic knowledge of ICH-GCP guidelines, DCGI and FDA regulatory guidelines, Schedule Y regulations, and medical terminology.
    • Great growth opportunities in the medical and health data field.
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    • A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring participant safety and protocol compliance.
    • Great growth opportunities in the medical and health data field.
    • Annotate and label medical, dietary, and nutrition-related data accurately.
    • Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
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    • Assist in monitoring clinical trial sites and study activities.
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    • Design and execute clinical studies.
    • Basic knowledge of medical terminology.
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    • We are looking for dedicated and experienced professionals with a background in clinical research who are ready to take the next step in their career.
    • The Clinical Research Coordinator (CRC) will be responsible for coordinating and managing clinical research activities across multiple study sites.
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Job Post Details

Clinical Research Coordinator | Freshers - job post

Clinigoal
Remote
₹3,00,000 - ₹6,00,000 a year

Job details

Pay

  • ₹3,00,000 - ₹6,00,000 a year

Job type

  • Full-time

Benefits

Pulled from the full job description

  • Provident Fund

Full job description

We are looking for enthusiastic and driven Life Sciences graduates who are eager to begin their careers in clinical research. This opportunity is designed for freshers with a strong academic foundation who are ready to apply their knowledge in real-world settings.

As a Clinical Research Coordinator, you will be part of a dynamic clinical research team, supporting the execution and management of Phase I to Phase IV clinical studies. This role offers hands-on exposure, structured learning, and a clear pathway to build a career in the clinical research and healthcare industry.

Candidates with a solid understanding of GCP guidelines and a genuine interest in clinical trials will be well-suited for this role.

Key Responsibilities:

1. Assist in the coordination and execution of Phase I to Phase IV clinical trials
2. Support patient recruitment, screening, and scheduling of study visits
3. Maintain accurate and up-to-date study documentation in compliance with GCP guidelines
4. Collect, review, and enter clinical data into study databases and ensure data integrity
5. Coordinate with investigators, sponsors, and site staff for smooth study operations
6. Monitor study progress and track timelines, ensuring adherence to protocols
7. Assist in preparing reports, regulatory documents, and audit-ready files
8. Ensure proper handling, storage, and documentation of study materials and samples Skill(s) required.

Eligibility
1. Education: B.Sc, M.Sc, B.Pharm, M.Pharm, Nursing, Biotechnology, Microbiology, Life Sciences, BDS, BHMS, or BAMS (2024, 2025, or 2026 pass-outs)

2. Certification: Candidates with a certification or diploma in Clinical Research will be given preference

3. Experience: Freshers can apply; internship experience in Clinical Research is an added advantage, but not mandatory

4. Skills: Basic knowledge of ICH-GCP guidelines, DCGI and FDA regulatory guidelines, Schedule Y regulations, and medical terminology

Pay: ₹300,000.00 - ₹600,000.00 per year

Benefits:

  • Provident Fund

Work Location: Remote

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