Job Title

Hiring For:Multiple Leading MNCs Job Summary: We are hiring skilled and experiencedSAS Clinical Programmersto join our global teams working with leading pharmaceutical companies and CROs. As a SAS programmer, you will be responsible for supporting clinical trial data analysis, CDISC implementation, and regulatory submissions across various therapeutic areas. Key Responsibilities: Develop, validate, and maintainSDTM and ADaM datasets , tables, listings, and figures (TLFs). Support clinical trial data analysis as perCDISC 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 yearsof hands-on experience inSAS programmingin a clinical trial environment. Strong knowledge ofCDISC standards (SDTM, ADaM &TFL) . Experience working on Safety & Efficacy Experience working withPhase I–IV clinical trials . Proficient inBase 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 onglobal clinical trialswith Tier-1 pharmaceutical clients. Competitive compensation and benefits. Flexible work models (remote/hybrid/on-site). Professional growth, training, and development support.