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Posted 1 weeks agoAssociate Director Biostatistician Consultant - Remote (24 months contract)
at ClinChoice
United StatesOn-site
Requirements
- 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
- 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
- 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.
- experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable.
- Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the
Additional details
- 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 Associate Director 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.
- This position will require minimal supervision from senior department staff and able to represent the Biostatistics function for complex studies or at project level. The position is responsible for working with study team members to independently 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
- 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 or project level meetings (if needed) are expected.
- requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.