Key Responsibilities

• Provide expertise to design, analysis & reporting of clinical trials & scientific research studies.
• Independently develop protocols & statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation.
• Collaborate with Statistical Programming to ensure delivery of high-quality outputs according to agreed-upon timelines.
• Develop strategy for data presentation & inference.
• Work collaboratively with multifunction teams in publication of scientific research.
• Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided.