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Medpace hiring Clinical Database Programmer in Mumbai. Life Sciences grads, Pharma\/CRO experience preferred. Apply now for growth opportunities.<\/p>\n
Join Medpace as a Clinical Database Programmer<\/strong> in Mumbai and be part of a global CRO driving innovation in clinical research. This role offers hands-on experience in programming, validation, and data management for critical clinical trials. If you are detail-oriented, skilled in Rave or Veeva EDC, and want to advance your career in Pharma\/CRO, this position is designed for you.<\/p>\n Medpace<\/strong> is a full-service global clinical contract research organization (CRO) providing Phase I-IV clinical development services to biotechnology<\/a>, pharmaceutical, and medical device industries. With over 30 years of experience, Medpace is committed to accelerating the development of safe and effective medical therapeutics through scientific and disciplined approaches.<\/p>\n Key Highlights:<\/strong><\/p>\n Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries<\/p>\n<\/li>\n Expertise across major therapeutic areas: oncology, cardiology, metabolic disease, CNS, anti-viral, anti-infective<\/p>\n<\/li>\n Recognized by Forbes as one of America\u2019s Most Successful Midsize Companies (2021-2024)<\/p>\n<\/li>\n Recipient of CRO Leadership Awards from Life Science Leader magazine<\/p>\n<\/li>\n<\/ul>\n Medpace values people, purpose, and passion<\/strong>, fostering an inclusive environment where employees contribute to advancing patient health globally.<\/p>\n As a Clinical Database Programmer<\/strong>, you will work closely with the Biometrics and Data Management teams to ensure accurate, high-quality clinical trial databases that meet regulatory and company standards.<\/p>\n Key Responsibilities:<\/strong><\/p>\n Develop, program, validate, and maintain clinical trial databases<\/p>\n<\/li>\n Maintain and enhance the company library of CDASH-compliant CRFs<\/p>\n<\/li>\n Serve as the primary technical contact for assigned studies with the Data Management team<\/p>\n<\/li>\n Ensure adherence to company standards and quality expectations in all programming tasks<\/p>\n<\/li>\n Troubleshoot and resolve database issues efficiently<\/p>\n<\/li>\n Support clinical operations and cross-functional teams to meet study timelines<\/p>\n<\/li>\n<\/ul>\n Technical Requirements:<\/strong><\/p>\n Strong proficiency in Medidata Rave study build or Veeva EDC systems<\/p>\n<\/li>\n Experience with custom functions using C# programming is preferred<\/p>\n<\/li>\n Certified Medidata Rave Study Builder certification is a plus<\/p>\n<\/li>\n Meticulous attention to detail to ensure database integrity and compliance<\/p>\n<\/li>\n<\/ul>\n Educational Requirements:<\/strong><\/p>\n Bachelor\u2019s or Advanced Degree in Life Sciences, Computer Science, or related field<\/p>\n<\/li>\n Courses: BSc. (Biology, Biotechnology, Microbiology), B.Tech (Bioinformatics<\/a>), MSc. (Life Sciences, Biostatistics), BCA, MCA<\/p>\n<\/li>\n<\/ul>\n Experience Requirements:<\/strong><\/p>\n Prior experience in clinical database programming in Pharma, Biotech, or CRO environment<\/p>\n<\/li>\n Hands-on experience with Rave or Veeva EDC systems<\/p>\n<\/li>\n Knowledge of CDASH standards and clinical data management processes<\/p>\n<\/li>\n<\/ul>\n Skills & Competencies:<\/strong><\/p>\n Strong verbal and written communication skills<\/p>\n<\/li>\n Excellent analytical, problem-solving, and organizational skills<\/p>\n<\/li>\n Ability to work independently and collaboratively in a fast-paced clinical research environment<\/p>\n<\/li>\n Familiarity with regulatory compliance requirements for clinical data<\/p>\n<\/li>\n<\/ul>\n Location:<\/strong> Navi Mumbai, Maharashtra, India
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Work Type:<\/strong> Full-time, office-based<\/p>\n
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