Clinical Data Programmer Role at Novotech | Pharmacy Graduates Eligible
A rare chance for early-career professionals to step into the field through this Novotech Clinical Data Programmer opportunity in Bangalore. The organization is seeking candidates with 6 months to 2 years of SDTM programming experience and a relevant educational background in life sciences or quantitative disciplines.
About Novotech
Novotech is a global full-service clinical Contract Research Organization (CRO) that specializes in providing comprehensive services in the clinical research sector. With a focus on Biometrics, Novotech operates in areas such as data management, statistical programming, biostatistics, and pharmacometrics. The organization is committed to delivering high-quality services that adhere to regulatory submission standards, including SDTM and ADaM datasets.
Job Details:
Company: Novotech
Job Role: Clinical Data Programmer I (SDTM)
Job ID: 4465
Job Type: Full Time
Location: Bangalore, Karnataka
Qualification: Bachelor’s Degree
Eligible Fields: Life Sciences / Computer Science / Mathematics / Statistics / Quantitative or Analytical Fields
Experience: 6 Months–2 Years in SDTM Programming
Key Skills: SAS, SDTM, CDISC, SDTMIG, Pinnacle 21, Define.xml
Industry: Clinical Research / CRO / Pharmaceutical
Posting Date: 31 August 2026
Novotech lists its Bangalore office at Ground Floor, Unit 1, Block E, Helios Business Park, Bangalore 560103, India.
About the Novotech Clinical Data Programmer I (SDTM) Role
In this Novotech Clinical Data Programmer role, the incumbent is responsible for SDTM programming based on clinical protocols, electronic Case Report Forms (eCRFs), and Statistical Analysis Plans (SAPs). The Clinical Programmer collaborates with biostatisticians, statistical programmers, and other clinical project stakeholders to transform raw clinical trial data into high-quality, standardized CDISC SDTM datasets. The position may also involve preparing data submission packages and supporting documentation for clients and regulatory authorities.
Key Responsibilities
- Performing SDTM programming and SDTM CRF annotation.
- Programming and validating datasets from raw clinical data into SDTM format.
- Conducting SDTM quality control, double programming, and peer reviews.
- Developing Define.xml, Reviewer’s Guides, and regulatory submission documents.
- Following statistical programming standards, conventions, and clinical data standards.
- Ensuring SAS programs are appropriately documented and traceable.
- Validating SAS datasets using Pinnacle 21.
- Maintaining clinical study documentation, programs, and project files.
Eligibility Criteria
Applicants should possess a Bachelor’s degree in Life Sciences, Computer Science, Mathematics, Statistics, or a Quantitative/Analytical field. Relevant educational backgrounds may include B.Pharm, B.Sc in various fields, BCA, B.Tech, B.E., and related degrees.
Required Skills
- SAS programming
- CDISC standards
- SDTM and SDTMIG
- Controlled terminology
- SDTM dataset creation and validation
- Clinical protocols
- Statistical Analysis Plans
- Pinnacle 21
Interested candidates can apply through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Novotech Clinical Data Programmer opportunity is ideal for those looking to advance their careers in clinical data programming. Candidates with the required qualifications and experience are encouraged to apply before the deadline to secure their chance to be part of a leading organization in the clinical research field.
