Were Hiring | Clinical Research Associate (CRA) at Reliance Lifesciences.

Location: Navi Mumbai

Experience: 4 -6 yrs

Employment Type: Full time

Key Responsibilities

- Participate in investigator recruitment and site evaluation visits.
- Conduct Site Initiation, Monitoring, and Study Close-out activities.
- Ensure compliance with ICH-GCP, study protocols, and applicable regulatory requirements.
- Perform source document review/verification and remote review of clinical trial data.
- Prepare monitoring reports and follow-up letters within defined timelines.
- Review protocols, CRFs/eCRFs, study manuals, and other study-related documents.
- Coordinate with investigators and site teams regarding Ethics Committee communication, site agreements, payments, and other administrative matters.





• Identify and escalate protocol deviations, compliance issues, and study-related risks.

Qualification Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field.

Desired Skills

Clinical Research | Clinical Trial Monitoring | CRA | ICH-GCP | Site Management | SIV | Monitoring Visits | Source Data Verification | CRF/eCRF | Protocol Compliance | Clinical Operations

Candidates with relevant clinical trial monitoring/site management experience are encouraged to apply.

Interested candidates can share their updated CV on [email protected]

📌 Clinical Research Associate (Navi Mumbai)
🏢 Reliance Life Sciences (RLS)
📍 Navi Mumbai