Experienced Clinical SAS Programmers looking for new opportunities in the clinical research and pharmaceutical industry can now apply for multiple openings across Mumbai, Pune, Hyderabad, Chennai, and Kolkata. Myriad Consulting is currently hiring professionals with strong expertise in Clinical SAS Programming, ADaM datasets, and TLF (Tables, Listings & Figures).
This opportunity is ideal for Clinical SAS professionals with 1โ10 years of experience who have worked on regulatory clinical trial programming and SDTM/ADaM deliverables. Candidates with relevant Clinical SAS Programming experience are encouraged to apply as soon as possible.
Clinical SAS Programmer Job Details
Job Title: Clinical SAS Programmer
Company: Myriad Consulting
Job Location:
- Mumbai
- Pune
- Hyderabad
- Chennai
- Kolkata
Work Mode: Hybrid (Currently)
Experience Required: 1โ10 Years
Industry: Clinical Research, Pharmaceutical, CRO
Key Responsibilities
- Develop and validate ADaM datasets according to CDISC standards.
- Generate Tables, Listings, and Figures (TLFs) for clinical studies.
- Perform Clinical SAS Programming for Phase IโIV clinical trials.
- Collaborate with biostatistics, data management, and clinical teams.
- Ensure programming deliverables meet regulatory requirements.
- Support submission-ready clinical datasets and outputs.
- Maintain programming documentation and quality standards.
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Statistics, Computer Science, or a related discipline.
- 1โ10 years of Clinical SAS Programming experience.
- Strong hands-on experience with ADaM datasets and TLFs.
- Good understanding of CDISC standards, clinical trial data, and regulatory programming.
- Excellent analytical and problem-solving skills.
Note: Freshers, interns, and candidates without Clinical SAS Programming experience will not be considered.
Preferred Skills
- Clinical SAS Programming
- Base SAS
- ADaM
- SDTM
- TLF Programming
- CDISC Standards
- Clinical Trial Programming
- Regulatory Submission Support
- Pharmaceutical Data Analysis
Benefits
- Hybrid work model.
- Opportunity to work on global clinical studies.
- Exposure to regulatory submissions.
- Career growth in Clinical SAS Programming.
- Collaborative work environment.
How to Apply
Interested and eligible candidates should share their updated resume to:
Email: sandeep.dalvi@myriadconsulting.co.in
Apply early, as applications will be reviewed on a rolling basis