Sr. Scientist, Statistical Programmer, Submission Data Standards Quality Management (Hybrid)
MerckHighlight
Summary
About the Role
About You
- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment.
- US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables.
- In-depth knowledge of industry clinical data standards (e.g., SDTM, ADaM) and submission deliverables.
- Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC).
- Experience using SAS, R, and Python to generate data-driven insights.
- Ability to complete statistical programming deliverables through the use of global outsource partner programming staff.
Benefits
- Comprehensive benefits package including medical, dental, and vision healthcare.
- Retirement benefits, including 401(k), paid holidays, vacation, and sick days.
- Eligibility for annual bonus and long-term incentive.
At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com. This site is intended for residents of the United States and Canada and their territories only. FLS: http://merck.us/3TKXNuZ