Skip to main content
Upload your CV and find your next job on Indeed!

Medical Sciences Research jobs

Sort by: -
    • Skills: Basic knowledge of ICH-GCP guidelines, DCGI and FDA regulatory guidelines, Schedule Y regulations, and medical terminology.
    • Develops and disseminate Requests for Proposals from Service Provider’s and will manage Service Providers including training and oversight, and serves as the…
    • Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
    • Infection control or patient monitoring research.
    • This position is ideal for someone who enjoys working *at the intersection of clinical research, medical…
    • Assist in monitoring clinical trial sites and study activities.
    • Ensure compliance with study protocols, GCP (Good Clinical Practice), and regulatory…
    • A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring participant safety and protocol compliance.
    • 1–4 years of experience in clinical research or clinical trial coordination.
    • Travel frequently to hospitals, clinics, and research sites across Kolkata and…
    • Scientific and medical literacy - demonstrates sufficient scientific/ medical knowledge to check pharmaceutical claims in promotional materials are referenced…
    • Basic knowledge of medical terminology.
    • Maintain accurate documentation and research records.
    • Maintain confidentiality of patient and research data.
    • 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.
    • Proven experience in reagent development for in vitro diagnostic (IVD) products or related industries (such as biopharma or medical devices).
    • Mentor junior research staff as the function grows.
    • Translate research findings into clinical, operational and marketting improvements.
    • Reviewing protocol and related documents.
    • Maintaining the database of the Investigator site.
    • Training investigator and related site staff on the study protocol.
    • Strong written and verbal communication skills, particularly in medical writing.
    • With deep domain expertise in regulatory sciences, clinical research solutions,…
    • Training in regulatory research methodologies.
    • Participate in internal discussions and present research outcomes.

People also searched:

medical scribe
medical writer
part time
research analyst
research assistant
research associate
work from home
analyst
assistant professor
biotechnology

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

Let Employers Find YouUpload Your Resume