Principal Statistical Programmer(SDTM/ADaM/TFLs)- ( /)

Principal Statistical Programmer(SDTM/ADaM/TFLs)- Hybrid (Hyderabad /Gurugram) Job Responsibilities 8+ years of relevant clinical/SAS/Statistical programming experience. All Principal level programmers to have SME level review capabilities as defined above. SP role (end to end) - Strong exposure to safety and efficacy programming, including end-to-end skills say CRF annotations, development of specifications SDTM/ADaM/TFLs, programming of SDTM/ADaM/TFLs, data management including Vendor data, handling e-submission tasks viz, DEFINE, SDRG ADRG. Proven track record of leading multiple clinical trials and demonstrating proactive project management skills. Lead experience of min 3 years. Excellent understanding of the clinical domain, CDISC standards, and experience across various(supported) therapeutic areas. Strong communication skills, problem-solving abilities, and ability to work collaboratively in cross-functional teams, in a dynamic environment. FSO experience is preferred. Clinical Phases: Phase-I,II,III, IV, except for dedicated Phase I exposure. TA: Oncology, Neurology, Or any TA. Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying. Principal Statistical Programmer(SDTM/ADaM/TFLs)- Hybrid (Hyderabad /Gurugram) Job Responsibilities 8+ years of relevant clinical/SAS/Statistical programming experience. All Principal level programmers to have SME level review capabilities as defined above. SP role (end to end) - Strong exposure to safety and efficacy programming, including end-to-end skills say CRF annotations, development of specifications SDTM/ADaM/TFLs, programming of SDTM/ADaM/TFLs, data management including Vendor data, handling e-submission tasks viz, DEFINE, SDRG ADRG. Proven track record of leading multiple clinical trials and demonstrating proactive project management skills. Lead experience of min 3 years. Excellent understanding of the clinical domain, CDISC standards, and experience across various(supported) therapeutic areas. Strong communication skills, problem-solving abilities, and ability to work collaboratively in cross-functional teams, in a dynamic environment. FSO experience is preferred. Clinical Phases: Phase-I,II,III, IV, except for dedicated Phase I exposure. TA: Oncology, Neurology, Or any TA. Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.