Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.
Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, creating the reporting database, and conducting the actual analysis once a reporting database is created.
Collaborate with data sciences in the planning and implementation of data quality assurance plans.
Effectively justify methods selected and implement previously outlined analysis plans.
Conduct peer-review of work products from statistical colleagues.
Maintain proficiency with respect to statistical programming and statistical methodology and in applying current and diverse methods.
Maintain current knowledge of CDISC data standards.
Effectively utilize current technologies and available tools for conducting the clinical trial analysis.

Communication of Results and Inferences
Collaborate with other statistical colleagues to write reports and communicate results.




Be responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.
Assist or respond to regulatory queries working in collaboration with other statistical colleagues

Therapeutic Area and Systems Knowledge
Understand relevant disease states and competitive landscapes to enhance the level of customer focus and collaboration.
Ensure replication of tools and systems, where applicable, and stay informed of technology advances.

Regulatory Compliance
Perform work in full compliance with assigned curriculum(s) and be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training

People Management and Development
Ensure all direct reports have a Performance Management (PM) and Development plan in place.
Conduct mid-year and final PM reviews to evaluate perfor

📌 Manager/senior Manager Bengaluru (India)
🏢 Eli Lilly
📍 India