Senior Biostatistician

Reporting to the Chief Statistician, this new position will provide high quality statistical design input and analyses for MediVector’s clinical trials and other statistical needs to meet project deliverables and timelines. Working collaboratively within a multidisciplinary team, the individual will use statistical knowledge and clinical research experience to investigate and propose statistical methodology, as well as to review appropriateness of methodology and conclusions from external sources.

 Responsibilities:

• Interact with team to provide statistical design of protocols
• Perform Sample Size calculations
• Create and review randomization plans and schedules
• Review and provide stat section of protocols
• Provide statistical input to Data Management efforts
• Develop Analysis Plans/Mock Data Presentations
• Perform statistical analyses of clinical trial data
• Summarize data and statistical findings for reports, submission, and conferences/publications     
• Provide direction & support to CROs for biostatistics
• Respond to project-level request for clarification of analyses from regulatory agencies

 Basic Qualifications:

• Ph.D. in statistics, biostatistics, or equivalent areas OR M.S. with 6+ years of relevant experience
• Must have 2-3 years scientific programming experience with SAS

Additional skills and preferences:

• Excellent interpersonal and organization skills
• Knowledge of the drug development process (phase I-IV)
• Ability to work independently and within a matrix team environment

Qualified candidates should submit resume with cover letter to James L. McEvoy at:  jmcevoy@medivector.com