Reliance Life Sciences is inviting applications for the position of Clinical Research Associate (CRA) in Navi Mumbai, Maharashtra. This full-time opportunity is suitable for experienced clinical research professionals with 4–6 years of experience in clinical trial monitoring, site management, and clinical operations.
Candidates holding a Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline can apply. The role involves investigator and site coordination, monitoring visits, source data verification, protocol compliance, and ensuring clinical trials are conducted according to ICH-GCP and applicable regulatory requirements.
Reliance Life Sciences CRA Job Overview
| Particulars | Details |
|---|---|
| Company | Reliance Life Sciences |
| Position | Clinical Research Associate (CRA) |
| Department | Clinical Research / Clinical Operations |
| Location | Navi Mumbai, Maharashtra |
| Employment Type | Full-time |
| Experience | 4–6 Years |
| Qualification | Bachelor’s/Master’s in Life Sciences, Pharmacy, Biotechnology or related field |
| Key Skills | CRA, ICH-GCP, Clinical Trial Monitoring, SDV, SIV, Site Management |
| Application Mode |
Key Responsibilities
The Clinical Research Associate at Reliance Life Sciences will be responsible for supporting and monitoring clinical studies while maintaining regulatory and protocol compliance. Major responsibilities include:
- Participate in investigator recruitment and clinical trial site evaluation visits.
- Conduct Site Initiation Visits (SIV), monitoring visits, and study close-out activities.
- Ensure study sites comply with ICH-GCP, clinical study protocols, SOPs, and applicable regulatory requirements.
- Perform source document review and Source Data Verification (SDV).
- Conduct remote reviews of clinical trial data where required.
- Prepare accurate monitoring reports and follow-up correspondence within defined timelines.
- Review clinical trial protocols, CRFs/eCRFs, study manuals, and other study-related documentation.
- Coordinate with investigators and clinical trial site teams.
- Support Ethics Committee communications, site agreements, payments, and administrative activities.
- Identify, document, and escalate protocol deviations, compliance issues, and study-related risks.
Qualification & Eligibility
Candidates interested in the Reliance Life Sciences Clinical Research Associate vacancy should have:
Educational Qualification:
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline.
Relevant qualifications may include B.Pharm, M.Pharm, B.Sc/M.Sc Life Sciences, B.Sc/M.Sc Biotechnology, and other closely related life-science degrees, subject to the employer’s assessment.
Experience:
Candidates should have approximately 4–6 years of relevant experience, particularly in clinical trial monitoring and/or clinical trial site management.
This vacancy is therefore intended primarily for experienced clinical research professionals rather than freshers.
Desired Skills
Candidates with expertise in the following areas will be particularly relevant:
Clinical Research | Clinical Trial Monitoring | CRA | ICH-GCP | Site Management | Site Initiation Visits | Monitoring Visits | Source Data Verification | CRF/eCRF | Protocol Compliance | Clinical Operations
Strong documentation, communication, investigator coordination, compliance monitoring, and risk-escalation capabilities are also important for this CRA position.
Why Consider This CRA Opportunity?
This position offers experienced clinical research professionals an opportunity to work across important aspects of clinical trial execution, including site initiation, monitoring, source data verification, investigator coordination, protocol compliance, and study close-out.
The role may be particularly relevant for professionals looking to strengthen their careers in clinical operations and clinical trial monitoring while gaining broader exposure to site and investigator management.
Note: Specific compensation, employee benefits, incentives, and other employment terms have not been provided in the recruitment information. Candidates should confirm these directly with Reliance Life Sciences during the recruitment process.
How to Apply
Eligible candidates can prepare an updated CV highlighting their clinical trial monitoring, site management, SIV, SDV, ICH-GCP, CRF/eCRF, and clinical operations experience.
Send your updated CV to:
Email: pradnya.kadu@relbio.com