Clinical Research Associate

Reliance Life Sciences (RLS); Navi Mumbai; On-site; INR 900,000 - 1,200,000; Full time

Job summary

Reliance Lifesciences in Navi Mumbai is seeking a Clinical Research Associate (CRA) with 4-6 years of hands-on experience to join our clinical operations team. You will participate in investigator recruitment and site evaluation visits, conduct Site Initiation, Monitoring, and Study Close-out activities, and ensure strict compliance with ICH-GCP and study protocols.

The role emphasizes monitoring data quality, source data verification, timely reporting, and proactive risk identification to

Qualifications

• Bachelor's or Master's in Life Sciences, Pharmacy, Biotechnology, or related field.
• Experience in clinical trial monitoring and site management.
• Knowledge of ICH-GCP guidelines.
• Excellent documentation and communication skills.

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 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 upscale protocol deviations, compliance issues, and study-related risks.

Education

Bachelor's/Master's degree in Life Sciences, Pharmacy, Biotechnology or related field

Job description

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 upscale 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.