Responsibilities
- Provide statistical support for Medical Affairs studies, including: Observational studies Real-world evidence (RWE) studies Post-marketing and Phase IV studies
- Contribute to study design, protocol development, and statistical analysis plans (SAPs)
- Perform and/or oversee statistical analyses and ensure accuracy and quality of outputs
- Collaborate with Medical Affairs, Clinical, Epidemiology, and HEOR teams
- Interpret study results and contribute to clinical study reports, publications, and presentations
- Ensure compliance with regulatory and internal standards
- Support publication strategy and scientific communication activities
- Mentor junior statisticians, if applicable
Requirements
- Master’s or PhD in Statistics, Biostatistics, or a related field
- 5–8+ years of relevant experience in the pharmaceutical, biotech, or CRO industry
- Strong experience in Medical Affairs / RWE / observational studies
- Proficiency in SAS and/or R
- Experience with study design, statistical modeling, and data interpretation
- Knowledge of regulatory guidelines and industry standards
Nice to Have
- Experience in Immunology / Oncology / relevant therapeutic area
- Prior experience supporting publications and external communications
- Strong stakeholder management and communication skills
Additional Information
- The Application Process: Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
