Principal Programmer, Oncology

🕒 April 15

🇮🇳 India – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 45%

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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Phastar

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2007

🏥 Healthcare

💼 Consulting

💊 Pharmaceuticals

Healthcare • Consulting • Pharmaceuticals

Phastar is a global biometrics contract research organization (CRO) that provides end-to-end clinical data solutions, including biostatistics, statistical programming, data management, data science, and data visualization to support clinical trials and regulatory submissions. The company offers flexible, scalable delivery models (project-based and functional service partnerships), proprietary frameworks and analytics tools to prepare high-quality, submission-ready data, and emphasizes a right-first-time approach and regulatory-first quality standards to accelerate drug development.

📋 Description

• Work as a principal programmer across multiple clinical and non-clinical studies • Supporting regulatory submission activities • Producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines • Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area • Producing, reviewing and updating complex dataset specifications (including efficacy) • Creating and debugging complex macros • Reviewing Statistical Analysis Plans (SAPs) • Ensuring the principles in the PHASTAR checklist are followed rigorously • Act as a Lead programmer on multiple studies and project, ensuring quality and timely delivery

🎯 Requirements

• Educated to BSc or above within Computer Science, Mathematics or a Science related discipline • SAS Programming Experience within the pharmaceutical industry and experience on Oncology Therapeutic Study • Good awareness of clinical trial issues, design, and implementation. • Experience of regulatory submissions and associated industry guidance • Familiarity with GCP and regulatory requirements • Knowledge of SDTM and ADaM CDISC standards

🏖️ Benefits

• PHASTAR is committed to the principles and practices of equal opportunities and to encouraging the establishment of a diverse workforce.