Associate Director Biostatistician Consultant (24 months contract)

ClinChoice

8h•CA$120,000 - CA$165,000

About The Position

ClinChoice is searching for an Associate Director Biostatistician Consultant to join one of our clients. This is a client-facing role requiring confidence and the ability to work independently while establishing a high-trust environment with the client’s counterparts. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and a supportive culture.

Requirements

MS or PhD in Statistics or Biostatistics
PhD + 6 years (or MS + 11 years) clinical trial experience in either a biotechnology or pharmaceutical company
Hands-on Phase I/II/III clinical trial experience
Proficient in SAS programming
Excellent oral and written communication skills

Nice To Haves

Excellence in R programming desirable
Previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable

Responsibilities

Work with study team members to independently contribute to the design of early/late-stage protocols across multiple therapeutic areas.
Help draft protocols or amendments.
Develop and write statistical analysis plans.
Perform statistical analyses for interim and final reports to be submitted to regulatory agencies.
Support submission activities, including design, analysis, and reporting of integrated summaries for safety and efficacy.
Attend and provide statistical contributions at study team meetings or project level meetings (if needed).
Contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers.