Role OverviewAs a Statistical Scientist, you will work globally and across a variety of therapeutic areas, leading complex studies and submissions, and developing protocols, review case report forms (CRFs), and develop analysis plans. You will also provide input or write specifications for tables and analysis files and communicate with clients regarding study protocol or statistical analysis issues as they arise.
What You Will Do
You will interpret analyses and write statistical sections of study reports, control costs and maximize revenue recognition, and run meetings, providing timeline updates and assessing resource needs.
Why It Might Be a Fit
You will have the opportunity to work globally and across a variety of therapeutic areas, with visibility at a team/site/staff level, and thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.
Requirements
- BS degree with 7 years of experience or MS degree with 5 years of experience OR equivalent experience
- Strong knowledge of complex statistical methods that apply to applicable clinical trials
- Experience in Early Clinical Development phases with Pharmacokinetic/Pharmacodynamic endpoints preferred
- Strong working knowledge of SAS and CDISC SDTM and ADaM
- Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics
Benefits
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance
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