SAS Clinical Programmer (5–10 Years Experience)-Immediate Joiner

Hiring For:

Job Summary:

SAS Clinical Programmers

Key Responsibilities:

• Develop, validate, and maintain

  SDTM and ADaM datasets

  , tables, listings, and figures (TLFs).
• Support clinical trial data analysis as per

  CDISC standards

  .
• Work closely with biostatisticians and data managers to ensure data quality and integrity.
• Write and validate SAS codes as per project and regulatory requirements.
• Prepare documentation for programming specifications and validation.
• Participate in project meetings, timelines discussions, and status updates.

Qualifications:

• 5 to 10 years

  of hands-on experience in

  SAS programming

  in a clinical trial environment.
• Strong knowledge of

  CDISC standards (SDTM, ADaM &TFL)

  .
• Experience working on Safety & Efficacy
• Experience working with

  Phase I–IV clinical trials

  .
• Proficient in

  Base SAS, SAS/SQL, SAS/Macro

  .
• Familiarity with regulatory requirements (e.g., FDA, PMDA).
• Excellent problem-solving and communication skills.

Preferred:

• Experience in working with global clients or MNCs.
• Exposure to tools like Pinnacle21, or other data review tools.
• Prior experience with submission-ready deliverables for FDA or EMA.

What We Offer:

• Opportunities to work on

  global clinical trials

  with Tier-1 pharmaceutical clients.
• Competitive compensation and benefits.
• Flexible work models (remote/hybrid/on-site).
• Professional growth, training, and development support.