Work as a data operations programmer on clinical and non-clinical trials; develop and maintain trial specific databases, including eCRF’s and edit checks using relevant programming languages of various levels of complexity to excellent quality whilst adhering to deliverable timelines. Support the programming of reports and listings which contribute to the standardization of process and reports used for data review and analysis for external partners/vendors. Support the development and maintenance of CDASH compliant therapeutic area and global eCRF libraries ensuring efficient mapping to current SDTM standards. Good knowledge of CDISC, CDASH and SDTM implementation guidelines. Excellent teamwork ethos, willingness to help others and learn new skills from working in a team environment.
Responsibilities
- Develop and maintain trial-specific databases, including eCRFs and edit checks, using relevant programming languages
- Deliver programming work of varying complexity to an excellent standard within agreed timelines
- Support the programming of reports and listings that contribute to the standardization of processes and reports used for data review and analysis by external partners and vendors
- Support the development and maintenance of CDASH-compliant therapeutic area and global eCRF libraries, ensuring effective mapping to current SDTM standards
- Work collaboratively within the team, support colleagues, learn new skills, and highlight risks to timelines or workload issues promptly
Qualifications
- Medidata Rave build experience, including eCRFs, edit checks, and migrations
- C# programming experience, including custom functions
- Good knowledge of CDISC, CDASH, and SDTM implementation guidelines
- Strong teamwork ethos, willingness to help others, and ability to learn new skills in a team environment
- Ability to identify and communicate risks to timelines and workload issues
Preferred:
· SAS programming
· Medrio and Viedoc experience
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📌 Data Operation Programmer (India)
🏢 PHASTAR
📍 India
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