Manager, Global Biostatistics and Programming

🕒 vor 1 Monat

🌲 North Carolina – Remote

info

💵 $132.900 - $199.400 / Jahr

⏰ Vollzeit

🟠 Senior

🔴 Experte

👔 Manager

🦅 H1B-Visum-Sponsor

info

🗣️🇺🇸🇬🇧 Englisch erforderlich

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Logo of Teleflex

Teleflex

10.000+ Mitarbeiter

⚕️ Krankenversicherung

💊 Pharmazie

💰 €275.000 Venture Round im 2010-01

Healthcare Insurance • Medical Devices • Pharmaceuticals

Teleflex ist ein globaler Anbieter von innovativen Medizinprodukten und -lösungen, der sich der Unterstützung von Gesundheitsfachkräften und der Verbesserung der Patientenversorgung widmet. Mit einem vielfältigen Portfolio, das Produkte für Anästhesie, Notfallmedizin, interventionelle Kardiologie und mehr umfasst, zielt Teleflex darauf ab, die Gesundheit und Lebensqualität zu verbessern. Das Unternehmen betont sein Engagement für Bildung und Kundensupport im Gesundheitswesen.

Beschreibung

• 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 • Provide strategic input during controlled clinical trial and real-world study protocol development and publication planning and execution • Manage work and consultants who are directly responsible for biostatistics input, support, and guidance; as well as strategic analysis and programming activities • Perform interim analyses and monitor the quality of data management deliverables during clinical trial execution • Cultivate a plan for sustaining biostatistics and programming for the Interventional Urology business unit • Manage external contractors/consultants, ensuring timelines are met according to objectives and goals and/or data reporting needs • Represent Teleflex in a customer-facing position with high levels of professionalism, service, and ethics • Demonstrate initiative and critical thinking to identify, prioritize process and performance gaps • Build collaborations with Clinical and Medical Affairs teams to align biostatistical analysis with global evidence generation plans

🎯 Anforderungen

• 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, clinical, or academic research setting required • Minimum of 3 years working on projects, including Urology therapies • Minimum of one year of prior experience managing/leading other team members or consultants • SAS Expertise required; certification preferred • Strong knowledge of US and international clinical regulations and guidance • Strong computer skills in Microsoft Office; high proficiency using electronic data capture systems and off-the-shelf data software • Ability to prioritize analytical deliverables through stakeholder management and negotiate timelines as needed • Ability to make independent decisions and take ownership within a fast-moving environment • Excellent organizational skills and attention to detail • Excellent verbal and written communication skills, including presentation skills • Ability to collaborate effectively and participate in a team environment • Ability to travel up to 5-10% of the time. Overnight and international travel may be required.

🏖️ Vorteile

• medical, prescription drug, dental and vision insurance • flexible spending accounts • participation in a 401(k) savings plan • various paid time off benefits, such as PTO, short- and long-term disability, and parental leave

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