Clinical SAS Programmer Hiring at Synergen Bio | Pune

Are you an experienced SAS programmer looking to advance your career in clinical research? Synergen Bio, a leading name in the biotech and pharmaceutical sector, is hiring Clinical SAS Programmers for their Pune office. This is a fantastic opportunity for individuals with a background in B.Pharm, MSc, or M.Pharm and 1-2+ years of experience to join a dynamic team. The position is based in Shivajinagar, Wakadewadi, Pune, and Synergen is looking for immediate joiners to be a part of their ongoing projects.

Key Responsibilities

As a Clinical SAS Programmer, you will be responsible for:

• SAS Programming in a CDISC Environment: Provide programming support in CDISC formats like SDTM and ADaM to ensure standardization and consistency in clinical trial data.
• Creating TLFs: Develop high-quality Tables, Listings, and Figures (TLFs) to present clinical trial results clearly and accurately.
• Data Checks and Complex Datasets: Write, modify, and maintain programs that handle complex datasets, safety and efficacy datasets, and perform data checks for thorough review.
• Project Documentation: Prepare and review essential project documentation such as Data Definition Tables and SDTM mapping annotations.
• Validation and Quality Control: Ensure validation, review of programs, and rigorous quality control on all outputs, adhering to Synergen’s corporate quality standards and ICH-GCP guidelines.
• Timely Deliverables: Collaborate with the team to ensure all timelines are adhered to and tasks are completed promptly without compromising quality.

Qualifications and Experience

To be eligible for the Clinical SAS Programmer position at Synergen Bio, candidates must meet the following criteria:

• Educational Background: A degree in B.Pharm, MSc, or M.Pharm in any relevant science discipline is required.
• Experience: A minimum of 1 to 2+ years of experience in SAS programming, particularly in the clinical research or pharmaceutical industry, is preferred.
• Skill Set: Candidates should have experience in CDISC standards, programming with SAS, and a strong understanding of clinical trial data management.
• Additional Preferences: Immediate joiners are highly encouraged to apply for this position, and familiarity with regulatory requirements and international standards will be an added advantage.

Work Location

This role is based in Shivajinagar, Wakadewadi, Pune.

How to Apply

If you meet the qualifications and are ready to take the next step in your career, Synergen Bio is eager to hear from you. Send your updated CV to careers@synergenbio.com to apply for the position.