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Lead Statistical Programmer
2 months ago
Job Title: Lead Statistical Programmer
Job Type: Full-time
Company: Warman O'Brien
Location: Hybrid / Home Based
Job Category: Data Science / Analytics
About Us: Warman O'Brien is a leading pharmaceutical company that thrives on a diverse company culture, celebrating the uniqueness of our employees and a commitment to inclusion. We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time and are proud to pursue the most promising science, wherever it might be found.
About the Role:
Key Responsibilities:- Accountable for statistical programming team delivery for 1 or more clinical projects of high complexity, scope, and/or criticality.
- Coordinate and oversee programming team activities and provide technical and project-specific mentorship to programming team members ensuring quality and on-time statistical programming deliverables in compliance with team processes and procedures.
- May act as a section lead of programming activities supporting a clinical development program, compound, or submission.
- Develop detailed programming strategy, specifications, and plan the programming deliverables for a one or more clinical projects.
- Perform comprehensive review of, and provide input into, project requirements and documentation.
- Design and develop programs in support of complex clinical analysis and reporting activities.
- Apply technical and analytical expertise to develop and implement solutions for use on clinical projects leading to increased efficiency and quality.
- Contribute to departmental innovation and process improvement projects.
- Oversee statistical programming activities outsourced to third-party vendors adopting appropriate processes and methods to ensure their performance meets the agreed-upon scope, timelines, and quality.
- Bachelor's degree or higher and/or equivalent in computer science, mathematics, data science/analytics, or other relevant scientific field (or equivalent theoretical/technical depth).
- Extensive years programming experience with growing responsibility in a pharmaceutical/clinical trial environment.
- Expert knowledge of data structures and relevant statistical programming languages including SAS (required) R or Python (advantageous).
- Demonstrated experience planning and coordinating programming activities and leading teams and working with cross-functional stakeholders and teams.
- Working knowledge of relevant regulatory guidelines (e.g. ICH-GCP, 21 CFR Part 11)
- Demonstrated experience planning and coordinating complex programming strategy and activities with the ability to support multiple high-complexity tasks.
- Demonstrated experience leading programming teams to meet project timelines and goals.
- Open & transparent culture that works in a very collaborative, global environment
- Work at the forefront of innovation with a strong focus on the use of R & Python with extensive training offered.
- Highly competitive salary + annual bonus.
- Generous benefits package including pension, medical cover, dental cover, share scheme, life assurance, and EAP.
- Healthy work-life balance and flexible working hours.
- Home-based / Hybrid working.
- Excellent career advancement opportunities.
