- Bachelor s degree / Advanced degree in Life Sciences or Computer Science or equivalent
- . Certified Medidata Rave Study Builder preferred
- Custom function (C# Programming) experience is preferred
- . Min 5 years of Rave study build experience in a similar position in Pharma / Healthcare sector
- Develop, program, validate and maintain clinical trial databases according to company and industry standards;
- Maintain and contribute to company library of standard CDASH compliant CRFs ; and
- Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.
Responsibilities
- Develop, program, validate and maintain clinical trial databases according to company and industry standards;
- Maintain and contribute to company library of standard CDASH compliant CRFs ; and
- Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.
Qualifications
- Bachelor s degree/Advanced degree in Life Sciences or Computer Science or equivalent;
- Min 5 years of Rave study build experience in a similar position in Pharma/Healthcare sector;
- Custom function (C# Programming) experience is preferred;
- Certified Medidata Rave Study Builder preferred;
- Some Veeva EDC programming experience is a plus;
- Excellent verbal and written communication skills; and
- Meticulous attention to detail.
📌 Experienced Clinical Database Programmer (Hyderabad)
🏢 Medpace Clinical Research India
📍 Hyderabad
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.