Principal Biostatistician Consultant
New Jersey, United States of America
Contract
2 weeks ago
Visa Sponsor
Key skills
R
About this role
Role Overview
- Work with Biometrics director to manage one or more compounds/Indications in R&D for the entire life cycle.
- Responsible for all statistical aspects of the drug development and/or post-approval programs.
- Coordinate statistical and programming support and manage contractors/CROs when necessary.
- Serve as lead statistician for clinical studies and collaborate effectively with the study team members.
Requirements
- M.S. or Ph.D. (or equivalent) in Statistics or Biostatistics is required.
- Minimum 4 years (Ph.D.) or 8 years (M.S.) pharmaceutical industry experience
- Should possess experience interacting with regulatory agencies (e.g. FDA, MHRA or EMEA).
- Experience managing multiple projects/therapeutic areas.
- Experience in managing external vendors (e.g. contractors, CROs).
- Capability in working independently and lead one or multiple clinical studies.
Benefits
- Competitive salary
- Hybrid work arrangement
- Opportunities for professional development
- Access to a supportive culture