Senior Scientist, Statistical Programming
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Job summary
Merck & Co., Inc. in Rahway, NJ is seeking a Senior Scientist, Statistical Programming to support late-stage drug/vaccine development.
You will develop and execute analysis datasets, tables, listings, and figures across trials and regulatory submissions, while collaborating with statistics and other stakeholders to ensure timely, high-quality deliverables. The role requires a Master’s or Bachelor’s degree with SAS experience in clinical trials, CDISC/ADaM knowledge, and leadership capabilities.
Qualifications
- Master’s degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience OR Bachelor’s degree plus 5 years SAS programming experience in a clinical trial environment.
- Experience with CDISC and ADaM standards.
- Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH.
Responsibilities
- Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects.
- Develop and execute statistical analysis and reporting deliverables (datasets, tables, listings, figures) for trials and regulatory submissions.
- Design and maintain statistical datasets for multiple stakeholders across development, outcomes research and safety evaluation.
- Collaborate with statistics and project stakeholders to ensure timely, high-quality deliverables.
- Serve as statistical programming point of contact and knowledge holder through the product lifecycle.
- Apply advanced methodologies and tools to enable discovery, development, and regulatory approval of products.
- Lead one or more projects.
Skills
Education
Tools
Job description
Senior Scientist, Statistical Programming – Rahway, NJ:
- Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects.
- Be accountable for the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.
- Design and maintain statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.
- Act as a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high quality deliverables.
- Serve as the statistical programming point of contact and knowledge holder through the entire product lifecycle.
- Apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.
- Lead one or more projects.
- Must have a Master’s degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years experience in SAS programming in a clinical trial environment OR a Bachelor’s degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years experience in SAS programming in a clinical trial environment.
- Experience in CDISC and ADaM standards.
- Experience in designing and developing complex programming algorithms and ensuring process compliance and deliverable quality.
- Must possess expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH.
- Systems and database expertise.
- Must have ability to comprehend analysis plans which may describe methodology to be programmed.
- Have an understanding of statistical terminology and concepts; strategic thinking ability to turn strategy into tactical activities.
- Ability to design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices.
- Ability to anticipate stakeholder requirements.
- Familiarity with clinical data management concepts.
- Effective interpersonal skills and ability to negotiate and collaborate effectively.
- Written, oral, and presentation skills.
- Knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings) also required.
- Must be a project leader and possess ability to complete tasks independently at a project level.
- Ability to collaborate with key stakeholders.
Clinical Development, Clinical Trials, Computer Science, Data Management, Data Modeling, Global Health, Marketing, Numerical Analysis, Outcomes Research, Project Leadership, Stakeholder Engagement, Stakeholder Relationship Management, Statistical Analysis, Statistical Programming, Strategic Thinking, Waterfall Model, Working Independently
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Regular
Not Applicable
11/1/2026
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
- We offer a comprehensive package of benefits.
- Medical
- Dental
- Vision healthcare
- Other insurance benefits (for employee and family)
- Retirement benefits
- 401(k)
- Paid holidays
- Vacation
- Compassionate and sick days
- More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits
The salary range for this role is $117,000.00 - $184,200.00
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
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