Required Clinical Research Coordinator - B.Sc / M.Sc (Life Sciences), B.Pharm / M.Pharm, or related healthcare background

OrciVita Sciences & Research Pvt. Ltd. Is hiring Clinical Research Coordinator (CRC) – Bhubaneswar

About OrciVita:

OrciVita Sciences & Research Pvt. Ltd. is an established Site Management Organisation (SMO) working with reputed sponsors, CROs, and investigators across India. They are committed to high-quality, ethical, and compliant clinical research with strong expertise in documentation, patient management, and regulatory processes.

Why Join OrciVita?

-Opportunity to work on diverse clinical studies

-Professional growth in a structured SMO environment

-Exposure to reputed sponsors and CROS

-Supportive and experienced clinical operations team

Details are provided below

1. Organization: OrciVita Sciences & Research Pvt. Ltd.

2. Location: Bhubaneswar, Odisha

3. Position: Clinical Research

Coordinator (CRC)

4. Employment Type: Full-time

On-site

5. Experience Required: 1-4 years (Experienced candidates preferred)

6. Job Responsibilities:

a. Coordinate day-to-day clinical trial activities at the study site

b. Patient screening, recruitment, informed consent process, and follow-ups

c. Ensure adherence to ICH-GCP, protocol, and regulatory requirements

d. Maintain essential documents, source documents, and CRFs/eCRFs

e. Coordinate with investigators, sponsors, CROs, and ethics committees

f. Support site monitoring visits, audits, and inspections

g. Ensure timely reporting of AEs/SAEs and protocol deviations

7. Eligibility Criteria:

Educational Qualification: B.Sc / M.Sc (Life Sciences), B.Pharm / M.Pharm, or related healthcare background

8. Experience:

-Minimum 1 year experience as a Clinical Research Coordinator at a Clinical Research Coordinator at a site or SMO

-Sound knowledge of ICH-GCP and clinical trial processes

-Good communication, documentation, and coordination skills

-Ability to work independently at the site

9. Preferred Skills:

-Prior experience in hospital-based clinical trials

-Hands-on experience with regulatory documentation Patient-centric approach and attention to detail

-Ability to manage multiple studies simultaneously

10. How to Apply:

Interested candidates may send their updated CV to:

hrorcivita@gmail.com

With Subject Line: Application for CRC - Bhubaneswar

Click Here for Details

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