Lead Biostatistician, Real‑World Evidence & Phase IV

headcount AG; Basel; Hybrid; CHF 170.000 - 230.000; Vollzeit

Zusammenfassung

headcount AG in Basel area, Switzerland, is seeking an Associate Director of Biostatistics with a focus on Real‑World Evidence. You will lead statistical activities for Phase IV studies, observational studies and patient registries, while collaborating with Medical Affairs, Market Access and Data Management to generate robust evidence.

The role requires at least 8 years of biostatistics experience in pharma/biotech/CRO, strong SAS programming, and experience with R is highly desirable.

Qualifikationen

• At least 8 years of relevant biostatistics experience in pharma, biotech, or CRO.
• Strong hands‑on SAS programming experience; R knowledge is highly desirable.
• Experience with Phase IV studies and real‑world evidence.
• Ability to work independently and to communicate statistical concepts clearly to diverse audiences.
• Experience in small or mid‑size pharma/biotech environments.
• A degree in statistics, mathematics, epidemiology or related discipline.

Aufgaben

• Lead statistical activities for Phase IV studies, observational studies and patient registries.
• Contribute to study design, endpoint selection, sample size calculations and SAPs.
• Independently program, analyze and validate study data and outputs.
• Generate evidence for medical affairs, market access and reimbursement activities.
• Provide statistical input for manuscripts, abstracts and scientific presentations.
• Collaborate with internal teams and external partners to modernise methods and programming practices.

Jobbeschreibung

headcount AG in Basel area, Switzerland, is seeking an Associate Director of Biostatistics with a focus on Real‑World Evidence. You will lead statistical activities for Phase IV studies, observational studies and patient registries, while collaborating with Medical Affairs, Market Access and Data Management to generate robust evidence.

The role requires at least 8 years of biostatistics experience in pharma/biotech/CRO, strong SAS programming, and experience with R is highly desirable.