Clinical Data Programmer Vacancy at Novotech – Apply Now!
Are you an experienced Clinical Data Programmer (SDTM) looking for an opportunity to work with a leading global Contract Research Organization (CRO)? Novotech is hiring a Clinical Data Programmer I (SDTM) in India to support clinical data programming, SDTM development, and regulatory submissions. If you have expertise in SAS programming, SDTM mapping, and CDISC standards, this is your chance to contribute to cutting-edge clinical research and help bring life-changing treatments to market.
Overview of Novotech!
Novotech is a leading full-service Contract Research Organization (CRO) headquartered in Sydney, Australia, with a strong presence across 34 offices worldwide and a team of over 3,000 professionals. We specialize in clinical trial management across all phases and therapeutic areas, ensuring the highest standards of quality, compliance, and efficiency. With a commitment to scientific excellence and regulatory integrity, Novotech partners with pharmaceutical, biotech, and medical device companies to bring life-changing treatments to market. Join us and be part of a global organization that is shaping the future of clinical research.
Job Description:
Job Title: Clinical Data Programmer I (SDTM)
Location:
IndiaBrief Position Description:
The Clinical Programmer (SDTM) is primarily responsible for SDTM programming based on Clinical Protocols, eCRF, and Statistical Analysis Plans. They collaborate with project stakeholders to produce SDTM outputs aligned with the study design.
Minimum Qualifications & Experiences:
- Bachelor’s Degree in Life Sciences, Computer Science, Mathematics, Statistics, or related field.
- Experience in SAS, SDTM Programming, and working with Clinical Protocols and Statistical Analysis Plans.
- Previous SAS Programming Experience.
- Experience in the Pharmaceutical industry, CRO, or related field.
Responsibilities:
- SDTM Programming and annotation of SDTM CRF.
- SDTM Quality Control, Double Programming, and Peer Review.
- Develop Define.xml datasets, Reviewers Guides, and related regulatory documents required for submission.
- Adhere to company statistical programming standards, conventions, and data standards.
- Ensure that SAS programs are properly documented and traceable.
- Maintain study documentation, programs, and files within project files.
- Maintain timesheets.
- Participate in department meetings.
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