www.acad.jobs : academic jobs worldwide – and the best jobs in industry
                
     
Position: Director of Statistics
Institution: Barinthus Biotherapeutics
Location: United Kingdom
Duties: Oversee statistical powering and provide input into the design of Vaccitech clinical trials; Identify potential issues for clinical development programs and associated trials, and provide statistical expertise for relevant issues, as needed; Perform statistical review of protocols; case report forms (CRFs); clinical study reports (CSRs) and associated tables, listings, and figures (TLFs); Investigator’s Brochures (IBs); scientific manuscripts; and research studies; Oversee development of Statistical Analysis Plans (SAPs) and associated mock shells for protocols, and act as primary signatory; Manage statistical vendors, including contract, budget, and quality oversight; Act on behalf of Vaccitech at DSMB and SMC meetings, as needed; Provide input into blinding and randomization procedures; Review animal and research studies for statistical relevance and appropriate sample sizes; Review and approve trends in manufacturing reports, such as stability studies; Review qualification experiments that require statistical assessment
Requirements: Advanced degree in statistics and at least 20 years of experience; Excellent command of English and good communication skills; Fluent in SAS, and needed regulatory filing systems; Familiar with prophylactic vaccine and/or immune-oncology trial designs and toxicology studies; Expected Vaccitech norms of collegiality, integrity, and transparency
   
Text: Director of Statistics Oversee statistical powering and provide input into the design of Vaccitech clinical trials; Identify potential issues for clinical development programs and associated trials, and provide statistical expertise for relevant issues, as needed; Perform statistical review of protocols; case report forms (CRFs); clinical study reports (CSRs) and associated tables, listings, and figures (TLFs); Investigator’s Brochures (IBs); scientific manuscripts; and research studies; Oversee development of Statistical Analysis Plans (SAPs) and associated mock shells for protocols, and act as primary signatory; Manage statistical vendors, including contract, budget, and quality oversight; Act on behalf of Vaccitech at DSMB and SMC meetings, as needed; Provide input into blinding and randomization procedures; Review animal and research studies for statistical relevance and appropriate sample sizes; Review and approve trends in manufacturing reports, such as stability studies; Review qualification experiments that require statistical assessment Advanced degree in statistics and at least 20 years of experience; Excellent command of English and good communication skills; Fluent in SAS, and needed regulatory filing systems; Familiar with prophylactic vaccine and/or immune-oncology trial designs and toxicology studies; Expected Vaccitech norms of collegiality, integrity, and transparency
Please click here, if the job didn't load correctly.







Please wait. You are being redirected to the job in 3 seconds.