Associate Director Biostatistician

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

Associate Director, Biostatistics | Real‑World Evidence

Location: Basel area, Switzerland
Employment type: Permanent
Working model: Hybrid, minimum 50% on‑site

The Opportunity

Our client is a Swiss pharmaceutical company focused on developing and commercialising treatments for rare diseases.
They are looking for an experienced biostatistician to strengthen their internal expertise in Phase IV studies and real‑world evidence. You’ll combine strategic statistical input with hands‑on analysis and programming, working closely with Medical Affairs, Market Access and Data Management.

Key Responsibilities

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

Requirements

• At least 8 years of relevant biostatistics experience within pharma, biotech or a CRO.
• Strong experience in Phase IV studies and real‑world evidence.
• Experience working within a small or mid‑size pharmaceutical or biotechnology company.
• Strong hands‑on SAS programming skills; R experience is highly desirable.
• A relevant degree in statistics, mathematics, epidemiology or a related discipline.
• Ability to work independently and communicate statistical concepts clearly to different audiences.
• Experience in market access, HEOR, HTA or rare diseases would be an advantage.