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About the role
As a Clinical Database Programmer at our Core Labs team in Mumbai, India, you will be responsible for developing, programming, validating, and maintaining clinical trial databases according to company standards. You will also play a key role in maintaining and preparing data models such as electronic CRFs and programming editing checks. In addition, you will act as the primary programmer contact for the data management team, providing necessary technical support and ensuring the quality of programming while adhering to company standards. Key Responsibilities: - Develop, program, validate, and maintain clinical trial databases - Maintain and prepare data models such as electronic CRFs - Act as primary programmer contact for the data management team - Provide technical support and ensure quality of programming Qualifications Required: - Bachelor's degree required, preferably in a math or information science field - Ability to work effectively in a team environment with data managers, coordinators, statisticians, and programmers - Familiarity with programming languages such as C# and SQL preferred Medpace is a full-service clinical contract research organization (CRO) that offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and employing more than 5,000 individuals across 40+ countries, we provide a flexible work environment, competitive compensation and benefits package, structured career paths, company-sponsored employee appreciation events, employee health, and wellness initiatives. Medpace has been continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility. As a Clinical Database Programmer at our Core Labs team in Mumbai, India, you will be responsible for developing, programming, validating, and maintaining clinical trial databases according to company standards. You will also play a key role in maintaining and preparing data models such as electronic CRFs and programming editing checks. In addition, you will act as the primary programmer contact for the data management team, providing necessary technical support and ensuring the quality of programming while adhering to company standards. Key Responsibilities: - Develop, program, validate, and maintain clinical trial databases - Maintain and prepare data models such as electronic CRFs - Act as primary programmer contact for the data management team - Provide technical support and ensure quality of programming Qualifications Required: - Bachelor's degree required, preferably in a math or information science field - Ability to work effectively in a team environment with data managers, coordinators, statisticians, and programmers - Familiarity with programming languages such as C# and SQL preferred Medpace is a full-service clinical contract research organization (CRO) that offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and employing more than 5,000 individuals across 40+ countries, we provide a flexible work environment, competitive compensation and benefits package, structured career paths, company-sponsored employee appreciation events, employee health, and wellness initiatives. Medpace has been continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
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