Merck & Co, Inc

Senior Scientist, Statistical Programming

Merck & Co, Inc$117K — $184K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in a relevant field plus 3 years of SAS programming experience, or Bachelor's degree plus 5 years of SAS programming experience in a clinical trial environment.
  • Experience with CDISC and ADaM standards essential.
  • Proven skills in developing complex programming algorithms and maintaining quality compliance.
  • Expertise in SAS programming including data steps, procedures, and SAS/MACRO.
  • Ability to comprehend analysis plans and understand statistical terminology and concepts.
  • Familiarity with clinical data management and effective interpersonal skills to collaborate and negotiate. '
  • Project leadership skills with a track record of independent task completion.

Responsibilities

  • Support statistical programming activities for late-stage drug/vaccine clinical development.
  • Develop and execute statistical analysis and reporting deliverables for clinical trials and regulatory submissions.
  • Design and maintain statistical datasets for use by multiple stakeholders.
  • Collaborate with statistics and project stakeholders to ensure efficient execution of project plans.
  • Serve as the statistical programming point of contact throughout the product lifecycle.
  • Apply advanced methodologies and tools to aid the development and approval of medical drugs and vaccines.
  • Lead one or more projects, ensuring high-quality deliverables.

Benefits

  • Comprehensive healthcare benefits including medical, dental, and vision for employees and families.
  • Retirement benefits including a 401(k) plan.
  • Paid holidays and vacation time.
  • Compassionate and sick leave days.
  • Opportunity to earn an annual bonus and long-term incentives.
Full Job Description
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.


Requirements:
  • 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.


Required Skills:
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

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

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.

The salary range for this role is
$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: 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

Search Firm Representatives Please Read Carefully
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.

Employee Status:
Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:
Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:
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.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

Merck & Co, Inc Careers

Join the visionary team at Merck & Co, Inc, a global leader in healthcare dedicated to advancing the world of medicine. As part of our professional community, you'll find dynamic job opportunities that foster innovation and leadership across various fields. Merck & Co, Inc is not just a company; it's a place where you can make a difference.

Work You’ll Do

At Merck & Co, Inc, we are committed to improving global health through groundbreaking research and innovative healthcare solutions. Our team is at the forefront of developing new therapies and vaccines that significantly impact public health worldwide. By joining us, you will collaborate with some of the brightest minds in the industry, using your skills to contribute to projects that save and improve lives around the globe.

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Whether you're seeking an internship, a graduate opportunity, or a professional position, Merck & Co, Inc offers a range of career paths in environments that promote rapid professional growth and development. Explore job opportunities in research, digital transformation, manufacturing, and more, all while benefiting from a culture that supports diversity and inclusion.

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Merck & Co, Inc is an ideal environment for those who lead with curiosity and the drive to innovate. Our leadership is committed to fostering a culture where inventive thinking and collaboration are encouraged, making it a perfect place for professionals who seek to make an impact through their work.

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With Merck & Co, Inc, you are not just getting a job; you're gaining access to unparalleled career development opportunities. Enhance your skills through diverse training programs, workshops, and continuous learning courses designed to help you grow at every stage of your career.

Benefits and Culture

We understand that our employees are our greatest asset, which is why we offer competitive benefits designed to support the health and well-being of you and your family. From comprehensive health care coverage and retirement plans to flexible working conditions and wellness programs, our benefits package is designed to meet the diverse needs of our team members.

Join Our Team

Ready to advance your career at Merck & Co, Inc? Search open positions that match your skills and interests. We are continuously hiring and looking for passionate, creative, and solution-driven team players. Prepare your resume, sharpen your interview skills, and become part of a company that's dedicated to making a difference.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

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