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Reliance Life Sciences is inviting applications for the position of Clinical Research Associate (CRA)<\/strong> in Navi Mumbai, Maharashtra<\/strong>. This full-time opportunity is suitable for experienced clinical research professionals with 4\u20136 years of experience<\/strong> in clinical trial monitoring, site management, and clinical operations.<\/p>\n Candidates holding a Bachelor\u2019s or Master\u2019s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline<\/strong> 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<\/strong>.<\/p>\n The Clinical Research Associate at Reliance Life Sciences<\/strong> will be responsible for supporting and monitoring clinical studies while maintaining regulatory and protocol compliance. Major responsibilities include:<\/p>\n Candidates interested in the Reliance Life Sciences Clinical Research Associate vacancy<\/strong> should have:<\/p>\n Educational Qualification:<\/strong> Relevant qualifications may include B.Pharm, M.Pharm, B.Sc\/M.Sc Life Sciences, B.Sc\/M.Sc Biotechnology<\/strong>, and other closely related life-science degrees, subject to the employer\u2019s assessment.<\/p>\n Experience:<\/strong> This vacancy is therefore intended primarily for experienced clinical research professionals rather than freshers<\/strong>.<\/p>\n Candidates with expertise in the following areas will be particularly relevant:<\/p>\n 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><\/p>\n Strong documentation, communication, investigator coordination, compliance monitoring, and risk-escalation capabilities are also important for this CRA position.<\/p>\n 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<\/strong>.<\/p>\n The role may be particularly relevant for professionals looking to strengthen their careers in clinical operations and clinical trial monitoring<\/strong> while gaining broader exposure to site and investigator management.<\/p>\n Note:<\/strong> 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.<\/p>\n<\/blockquote>\n Eligible candidates can prepare an updated CV highlighting their clinical trial monitoring, site management, SIV, SDV, ICH-GCP, CRF\/eCRF, and clinical operations experience<\/strong>.<\/p>\n Send your updated CV to:<\/p>\n Email:<\/strong> pradnya.kadu@relbio.com<\/a><\/strong><\/p>\n<\/div>\nReliance Life Sciences CRA Job Overview<\/h2>\n
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\n Particulars<\/th>\n Details<\/th>\n<\/tr>\n \n Company<\/td>\n Reliance Life Sciences<\/td>\n<\/tr>\n \n Position<\/td>\n Clinical Research Associate (CRA)<\/td>\n<\/tr>\n \n Department<\/td>\n Clinical Research \/ Clinical Operations<\/td>\n<\/tr>\n \n Location<\/td>\n Navi Mumbai, Maharashtra<\/td>\n<\/tr>\n \n Employment Type<\/td>\n Full-time<\/td>\n<\/tr>\n \n Experience<\/td>\n 4\u20136 Years<\/td>\n<\/tr>\n \n Qualification<\/td>\n Bachelor\u2019s\/Master\u2019s in Life Sciences, Pharmacy, Biotechnology or related field<\/td>\n<\/tr>\n \n Key Skills<\/td>\n CRA, ICH-GCP, Clinical Trial Monitoring, SDV, SIV, Site Management<\/td>\n<\/tr>\n \n Application Mode<\/td>\n Email<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n Key Responsibilities<\/h2>\n
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Qualification & Eligibility<\/h2>\n
Bachelor\u2019s or Master\u2019s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline<\/strong>.<\/p>\n
Candidates should have approximately 4\u20136 years of relevant experience<\/strong>, particularly in clinical trial monitoring and\/or clinical trial site management.<\/p>\nDesired Skills<\/h2>\n
Why Consider This CRA Opportunity?<\/h2>\n
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How to Apply<\/h2>\n