Reliance Life Sciences (RLS) is recruiting for the Clinical Research Associate (CRA) position in Navi Mumbai. The role involves clinical trial monitoring, site management, regulatory compliance, source data verification, and coordination with investigators and clinical trial site teams.
Candidates with a bachelor’s or master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field and relevant clinical trial monitoring experience can apply.
Job Details
| Particulars | Details |
|---|---|
| Company | Reliance Life Sciences (RLS) |
| Job Role | Clinical Research Associate (CRA) |
| Location | Navi Mumbai, Maharashtra |
| Experience | 4–6 years |
| Employment Type | Full-time |
| Openings | 4 |
| Salary | ₹5 –13 LPA |
Key Responsibilities
- Participate in investigator recruitment and site evaluation visits.
- Conduct Site Initiation Visits (SIV), monitoring visits, and study close-out activities.
- Ensure compliance with ICH-GCP, study protocols, and regulatory requirements.
- Perform source document review, source data verification, and remote clinical data reviews.
- Prepare monitoring reports and follow-up letters within defined timelines.
- Review protocols, CRFs/eCRFs, study manuals, and related documents.
- Coordinate with investigators and site teams on Ethics Committee communications, site agreements, and payments.
- Identify and escalate protocol deviations, compliance issues, and study-related risks.
Eligibility and Qualifications
- Bachelor’s or master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field.
- 4–6 years of clinical trial monitoring or site management experience.
Required Skills
Clinical Research, Clinical Trial Monitoring, CRA, ICH-GCP, Site Management, Site Initiation Visits (SIV), Monitoring Visits, Source Data Verification, CRF/eCRF, Protocol Compliance, and Clinical Operations.
How to Apply
Interested candidates can share their updated CV via email.
Email: pradnya.kadu@relbio.com
Location: Navi Mumbai, Maharashtra
