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You will be updated with latest job alerts via emailSummary of Job Responsibilities: Work under the direction of Senior Biostatistician/Technical Lead especially on complex standard assignments. Understand client requests and needs Create SAS tables and graphs memos for CSRs safety reports headlines exploratory studies etc Interact with Chesterbrook statisticians for clarity of specifications data issues revision of reports etc. Perform validation of results Carry out statistical analysis as per the requirements in the protocol Ensure timely delivery of Products Adhere to quality standards (as specified by client(s) as applicable) Participate in training and mentoring of new recruits
Qualifications and Experience: M.Sc Statistics/Biostatistics with minimum 3year of experience in statistical programming with clinical data General knowledge of regulatory requirements and drug development process. Fair knowledge of Clinical trial domain and good SAS programming skills. Good English communication Base SAS certification
Full Time