Job Title

SUMMARYAs 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 domainsProgram complex non‑efficacy outputs and figuresDevelop, debug, and maintain complex SAS macrosCreate, QC, review, and update complex dataset specifications across single and multiple studiesIndependently review SAPs (simple study designs) and output shells, providing feedbackApply SDTM and ADaM standards consistently and correctlyLead the creation and delivery of Clinical Regulatory Trial (CRT) packages, including define.xml / define.pdfAct as a point of contact for programming issues and ensure team alignmentLiaise with Study Statisticians and Project Managers on resourcing and deliverablesTake ownership of study-level resources and timelinesSupport internal training and contribute to programming development initiativesEnsure compliance with SOPs, internal checklists, and documentation archiving standardsKEY EXPERTISE & COMPETENCIESStrong written and verbal communication skillsCollaborative team player with a positive, proactive mindsetStrong problem‑solving skills and attention to detailAbility to manage competing priorities and make timely technical decisionsStrong understanding of regulatory requirementsProactive in identifying and resolving study‑level issuesOpen to feedback and continuous improvementQUALIFICATIONSBachelor’s degree or above in Computer Science, Mathematics, or a related scientific discipline5+ years of experienceStrong SAS programming experience within the pharmaceutical industryExperience programming to CDISC SDTM and ADaM standardsSolid understanding of clinical trial design and implementationFamiliarity with GCP and regulatory requirementsExperience with FDA CRT delivery (define.xml, define.pdf)DURATIONContract (12-18 Months)SALARYAttractive hourly rateLOCATIONRemote (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 APPLYPlease click ‘apply’ or contact Joesela Alolod A. (Recruitment Sourcer) at Planet Pharma for more information: E: T: +61 370580550Linkedin: /in/joeselaaloloda/