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Strong CRO brand and Bangalore metro raise competition, though niche CDISC/RAVE skills limit candidate pool.
Highly specialized clinical trial standards and tools (CDISC, ADaM, RAVE) make cross-industry transfer difficult.
Explicit 7+ years, RAVE, CDISC, and SAS/R requirements create strict mandatory filters.
Lead design, development, and validation of clinical data science programming solutions for clinical trials.
Manage day-to-day clinical data science activities and provide technical leadership to the programming team.
Collaborate with biostatisticians, data managers, and clinical teams to create data specifications and analysis plans.
Bachelor's degree in life sciences, computer science, or a related discipline.
7+ years of experience with clinical data programming, including proficiency in SAS, R, or relevant programming languages.
In-depth knowledge of clinical trial data structures, CDISC standards (SDTM, ADaM), and regulatory requirements.
Willingness to travel approximately 10%; legal right to work in India (Bangalore) required.
Experienced in managing multiple projects and competing priorities within clinical data science programming.
Strong leadership capability demonstrated by mentoring junior programmers and guiding technical solutions.
Comfortable working in cross-functional teams with biostatistics, data management, and clinical functions.