SeniorManagerBiostatisticianConsultant

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for an Senior Manager Biostatistician Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Job Duties This position is responsible for working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies. The position will also support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy. Attendance and statistical contributions at study team meetings are expected. Within the BDM Department, leadership skills are needed to contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers. Qualification and Required Skills MS or PhD in Statistics or Biostatistics PhD +4 years (or MS +9 years) clinical trial experience in either a biotechnology or pharmaceutical company Hands-on Phase I/II/III clinical trial experience and proficient in SAS programming. Excellence in R programming desirable. Excellent oral and written communication skills. Although not required, previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we rece