Manager Global Biostatistics and Programming; REMOTE

Manager Global Biostatistics and Programming (REMOTE)

Teleflex is a global provider of medical technologies, driven by our purpose to improve health and quality of life. As a leading company, we strive to become the most trusted partner in healthcare. For more information, please visit .

The Manager, Global Biostatistics and Programming, is responsible for developing and implementing statistical analysis plans (SAPs) as well as producing the key clinical data outputs that align with the evidence generation needs across the organization. The role will be heavily relied upon to provide strategic input during controlled clinical trial and real‑world study protocol development and publication planning and execution (e.g., sample size calculation & justification).

As an integral member of the Medical Affairs team, this position manages work and consultants who are directly responsible for biostatistics input, support, and guidance; as well as strategic analysis and programming activities that serve as a critical foundation for publications, presentations, clinical protocols, clinical evaluation reports (CERs), and SAPs. During clinical trial execution, the function may be asked to perform interim analyses and monitor the quality of data management deliverables.

• Customer Experience – Representing Teleflex in a customer‑facing position is a tremendous responsibility and opportunity. All colleagues are expected to perform with the highest levels of professionalism, service, and ethics to strengthen the brand and relationship with our customers.
• Continuous Improvement – Demonstrates initiative and critical thinking to identify, prioritize process and performance gaps. Develops solutions to deliver improved results. Exemplifies continuous improvement, thought processes, and focus.
• Culture and Values – Exemplifies Teleflex values and ensures a fair, open, and productive climate that is engaging, ethical, and legally compliant. Strives to work effectively across boundaries in a complex matrix environment.
• Build collaborations with Clinical and Medical Affairs teams to align biostatistical analysis with global evidence generation plans, including but not limited to the following:
  • Long‑term evidence generation plans that yield appropriate datasets from which to make evidence‑based recommendations
  • Development and execution of SAPs and statistical analysis reports (SARs)
  • Programming of clinical data outputs for (but not limited to) publications, presentations, and CERs
  • Strategic input for collaborative research projects, clinical trial development, and real‑world study data
  • Determination and justification of study populations through sample size calculations (with written justifications to be included in protocols and manuscripts)
  • Further support of Clinical studies may include:
    • Aid ongoing study data quality through closeout and archival, including edit checks per data validation plan or data management plan
    • Review CRF annotations and data specifications and ensure CRFs meet the guidelines of the protocol

• Manage and coordinate all independent statistical contractors/consultants on multiple projects and timelines; ensure external requests are funneled through this function and prioritized accordingly.
• Write SAS programs to validate tables, listings, and figures, and analysis datasets.
• Utilize SAS programming skills to perform all programming required for clinical trial analysis and reporting.
• Ensure adherence and consistency per standard operating protocols.
• Produce ad‑hoc statistical outputs and reports for Clinical, Scientific, and/or Medical affairs teams.
• Perform other duties as requested.
• Contribute to the company culture of being collaborative, respectful, transparent, ethical, efficient, high achieving, and fun.

• Master’s degree in a quantitative discipline (e.g., statistics, operations research, bioinformatics, economics, computational biology, computer science, mathematics, physics, electrical engineering, industrial engineering) with at least 10 years of direct biostatistics and programming experience in a pharmaceutical, medical device,…