Overview

Work as a senior programmer on clinical and non-clinical trials; producing complex datasets and outputs to excellent quality whilst adhering to deliverable timelines. Good knowledge of CDISC SDTM and ADaM implementation guidelines; producing, reviewing and updating complex data specifications; creating and debugging complex macros; understanding Statistical Analysis Plans (SAPs) and output shells for day to day programming activities. Excellent team work ethos, willingness to help others and learn new skills from working in a team environment.

This role is full-time and fully remote. The successful candidate may be based in India or South Africa.

Responsibilities

The following areas of expertise will be aligned to the role...

• Statistical expertise and scientific leadership

• Leadership and people development

• Compliance, quality and governance

• Communication and influence

Qualifications

• Educated to BSc within Computer Science, Mathematics or a Science related discipline

• Strong SAS and R Programming Experience within the pharmaceutical industry





• A good awareness of clinical trial issues, design, and implementation

• Familiarity with GCP and regulatory requirements

• Experience with CDISC (SDTMs, ADaMs, P32, Define, Reviewers Guide)

• The successful candidate will be able to work remotely as part of a global team. This will occasionally require flexibility as to working hours

• Experience with R Shiny is advantageous

• Oncology experience is advantageous

• Late Phase experience is advantageous

• HTA/ HEOR experience is advantageous

• Solid communication skills are advantageous

• A Good understanding of GCP and GDPR principles is advantageous

• Educated to MSc within Computer Science, Mathematics or a Science related discipline is advantageous

Why Join Us

• Remote working and flexible working hours

• Career development, mentorship, and continuous learning

• Supportive, friendly, and cooperative culture

About Phastar

Phas

📌 Senior Programmer (India)
🏢 PHASTAR
📍 India