Senior Scientist, Statistical Programming
Merck · Rahway, NJ
BiometricsFull-time$117k–$184kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Scientist, Statistical Programming role supporting late-stage clinical development and regulatory submissions for drugs and vaccines. Responsible for developing statistical analysis datasets, tables, and figures while collaborating with cross-functional teams throughout the product lifecycle.
What they're looking for
- Expertise in SAS including data steps, procedures, macros, and graphics for clinical trial programming
- Experience with CDISC and ADaM standards
- Knowledge of statistical databases, data management concepts, and analysis plan comprehension
- Demonstrated ability to design complex programming algorithms and ensure process compliance
- Strong interpersonal, presentation, and written communication skills
- Project leadership capability and ability to work independently
What you'll be doing
- Develop and execute statistical analysis and reporting deliverables for clinical trials and regulatory submissions
- Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation
- Collaborate with statistics teams and stakeholders to ensure efficient execution and timely quality deliverables
- Lead one or more projects and serve as statistical programming point of contact throughout product lifecycle
- Apply scientific methodologies and tools to support drug and vaccine discovery, development, and regulatory approval
Privacy & handoff
This role links to Merck's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.