We are seeking a Biostatistician Consultant for a biopharmaceutical client for a 6-month (initially) contract. This is an exciting opportunity for a seasoned professional to provide strategic biostatistical expertise and oversight across multiple clinical studies.
Location: Leiden or Mechelen, 2 days on-site per week Contract: 6 months Start Date: ASAP
Key Responsibilities
Provide biostatistical support to Clinical Study Teams in design, analysis, and reporting of clinical trials
Develop Statistical Analysis Plans and provide input on study design including sample size calculations
Coordinate with External Service Providers for biostatistical activities and deliverables
Review regulatory documents including protocols and Clinical Study Reports
Execute interim analyses and produce topline results and CSR outputs
Support regulatory submissions and ensure compliance with ICH-GCP guidelines
Qualifications and Experience
5+ years of experience as a Statistician in the pharmaceutical industry, ideally with a focus on Oncology
Master's degree in Statistics or related field
Experience in clinical biostatistics with SAS or R proficiency
Knowledge of regulatory guidelines (ICH-GCP)
Experience working with external service providers
Can this role be interesting for you or anyone you know? If so, please send your CV and contact information to d.sonneveld@panda-int.com, and we will be in touch for a conversation.