Job Title: Associate Director Biostatistics
Location: Fully Onsite in Maryland
Company: Pharma
Therapeutic Area: CNS
Qualifications:
- PhD in Statistics or Biostatistics
- 4+ years of Clinical Trial Experience
- Programming Skills: SAS, and R/S Language
- Ability to work cross-functionally between departments.
*Must have 4+ years of relevant experience within the pharmaceutical / CRO industry*
Responsibilities:
- Provide in-depth knowledge of clinical trials methodology, regulatory requirements, and statistics.
- Provide Mentorship to junior biostatisticians
- Collaboration and Communication: Collaborate and work cross-functionally among Statistical Programmers, Clinical Data Managers, Clinical Teams, and Regulatory Affairs to develop data analysis plans and ensure alignment on reporting.
- Participate in and contribute to regulatory submissions and respond to regulatory queries as needed
- Stay updated about industry trends and advancements in statistical programming techniques and software
- Lead and ensure the accuracy, consistency, and completeness of statistical outputs.
They are looking to fill this role urgently, so if you are open to relocating / reporting onsite, please apply in!
