Clinical Research Associate

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 removed]