SUMMARY As a Senior Programmer, you will work across clinical and non‑clinical trials, delivering high‑quality programming outputs within agreed timelines. You will apply deep knowledge of CDISC SDTM and ADaM, interpret SAPs and output shells, develop macros, and support study‑level programming leadership. You’ll also act as a key technical contact, supporting junior team members and influencing best practices across studies. RESPONSIBILITIES Program and validate SDTM datasets, including complex efficacy and laboratory domains Program complex non‑efficacy outputs and figures Develop, debug, and maintain complex SAS macros Create, QC, review, and update complex dataset specifications across single and multiple studies Independently review SAPs (simple study designs) and output shells, providing feedback Apply SDTM and ADaM standards consistently and correctly Lead the creation and delivery of Clinical Regulatory Trial (CRT) packages, including define.xml / define.pdf Act as a point of contact for programming issues and ensure team alignment Liaise with Study Statisticians and Project Managers on resourcing and deliverables Take ownership of study-level resources and timelines Support internal training and contribute to programming development initiatives Ensure compliance with SOPs, internal checklists, and documentation archiving standards KEY EXPERTISE & COMPETENCIES Strong written and verbal communication skills Collaborative team player with a positive, proactive mindset Strong problem‑solving skills and attention to detail Ability to manage competing priorities and make timely technical decisions Strong understanding of regulatory requirements Proactive in identifying and resolving study‑level issues Open to feedback and continuous improvement QUALIFICATIONS Bachelor’s degree or above in Computer Science, Mathematics, or a related scientific discipline 5+ years of experience Strong SAS programming experience within the pharmaceutical industry Experience programming to CDISC SDTM and ADaM standards Solid understanding of clinical trial design and implementation Familiarity with GCP and regulatory requirements Experience with FDA CRT delivery (define.xml, define.pdf) DURATION Contract (12-18 Months) SALARY Attractive hourly rate LOCATION Remote (India) ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. TO APPLY Please click ‘apply’ or contact Joesela Alolod A. (Recruitment Sourcer) at Planet Pharma for more information: E: T: Linkedin:
Job Title
Senior & Principal Programmers