Principal Statistical Programmer

Job not on LinkedIn

🕒 March 17

🇮🇳 India – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 55%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Develop and validate SDTM/ADaM datasets and TLFs • Prepare specifications and generate Define.XML, ADRG, and SDRG • Support safety and efficacy analyses • Contribute to e-submissions and ensure CDISC compliance • Collaborate with cross-functional teams across studies • Lead clinical study trials • Lead multiple clinical trials and apply proactive project management skills • Support clinical studies across Oncology, Neurology, or other therapeutic areas

🎯 Requirements

• 8+ years of relevant clinical/SAS/Statistical programming experience • Prefer to have SME-level review capabilities at an experienced Senior-level profile • Experience developing and validating SDTM/ADaM datasets and TLFs • Experience preparing specifications and generating Define.XML, ADRG, and SDRG • Experience supporting safety and efficacy analyses • Knowledge of e-submissions and CDISC compliance • Proven track record leading multiple clinical trials • Proactive project management skills • Minimum 1+ year of lead experience • Excellent understanding of the clinical domain and CDISC standards • Experience across various supported therapeutic areas • Strong communication and problem-solving abilities • Ability to work collaboratively in cross-functional teams and a dynamic environment • Experience with Clinical Phases I, II, III, and IV, except for dedicated Phase I exposure • Therapeutic area experience in Oncology, Neurology, or any therapeutic area • Equivalent experience, skills, and/or education may be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations, when appropriate, for employees or applicants with disabilities