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    • Assist in the coordination and execution of Phase I to Phase IV clinical trials.
    • Collect, review, and enter clinical data into study databases and ensure data…
    • Write protocols, amendments, case record forms, clinical reports and other documents relevant for dedicated clinical investigations.
    • Coordinate day-to-day clinical trial operations at the site.
    • A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring…
    • Translate research findings into clinical, operational and marketting improvements.
    • This role runs the clinic's research pipeline end-to-end — from data…
    • Required clinical research associates with prior experience of 3 years plus in similar position.
    • Checking documents of CRO internal System audit at specified…
    • 1–4 years of experience in clinical research or clinical trial coordination.
    • The Clinical Research Coordinator (CRC) will be responsible for coordinating and…
    • A CRA ensures that clinical trials are conducted ethically, safely, and in strict compliance with the study protocol and regulatory standards like *Good…
    • We are looking for a sincere, disciplined, and confident communicator to coordinate with hospitals for clinical validation projects, ensure timely follow-ups,…
    • Coordinate and manage clinical trial activities.
    • Recruit and screen study participants.
    • Obtain informed consent from participants.
    • Substantial start up experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
    • This is an excellent opportunity for life science graduates who want to start their career in clinical trials and clinical research operations.
    • 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.
    • MSc Life Sciences / Biotechnology with clinical research experience.
    • Strong scientific understanding and clinical research methodology.
    • Assist in monitoring clinical trial sites and study activities.
    • Ensure compliance with study protocols, GCP (Good Clinical Practice), and regulatory…
    • Stay informed about industry trends and advancements in clinical research.
    • To facilitate and coordinate the all daily clinical research trial activities, for…

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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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