you will be responsible for: Designing statistical strategies and providing guidance throughout various phases of drug development Developing study protocols Conducting data analysis using
SAS software Interpreting results and communicating findings with cross-functional teams Contributing towards regulatory submissions Overseeing statistical aspects of trials Providing mentorship and leadership to … research/pharmaceuticals domain/Phase 3 Excellent knowledge of relevant regulations including ICH-GCP guidelines Proficiency with programming languages such as R/
SAS/Python Strong communication skills, both written & verbal; ability to influence stakeholders at all levels Experience in oncology, knowledge of endpoints, and proficiency in …
SAS (Candidates with a strong background in statistics in other therapy areas also considered) Desired skills: Survival analysis, MMRM models, binary endpoints Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity
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