Senior Scientist Statistical Programming, Late-Stage (Hybrid)
Company websitemerck.com (Merck & Co., opens in new tab)
Base salary $117,000 to $184,200
Employer-published annual base salary, USD. Advertised base range in North Wales, PA +1 more
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationNorth Wales, PA +1 more
- WorkplaceHybrid
- Status at last checkSource accepting applications when checked
- Last checked (1 h ago) · observed since
All places named
- North Wales, PA
- Rahway, NJ
About this job
Job Description
In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, 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.
This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more projects. Accountability predominantly includes 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.
The incumbant is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.
The position is a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high quality deliverables.
For assigned projects the position serves as the statistical programming point of contact and knowledge holder through the entire product lifecycle.
Primary Activities:
- Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices.
- Maintain and manage a project plan including resource forecasting.
- Coordinate the activities of a global programming team that includes outsource provider staff.
- Membership on departmental strategic initiative teams.
Skills:
Education and Minimum Requirement:
- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environment.
- MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 3 years SAS programming experience in a clinical trial environment.
Department Required Skills and Experience:
- Effective interpersonal skills and ability to negotiate and collaborate effectively.
- Effective written, oral, and presentation skills.
- Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings).
- A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders.
Position Specific Required Skills and Experience:
- Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.
- Designs and develops complex programming algorithms.
- Ability to comprehend analysis plans which may describe methodology to be programmed; an understanding of statistical terminology and concepts.
- Familiarity with clinical data management concepts.
- Experience in CDISC and ADaM standards.
- Experience ensuring process compliance and deliverable quality.
- Strategic thinking - ability to turn strategy into tactical activities; 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.
Preferred Skills and Experience:
- Experience with GenAI tools (e.g R, R Shiny, R Force, Python Claude etc) is highly preferred.
- Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC).
- US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables.
- Experience assuring programming consistency across protocols and projects, directing the program development effort of other programmers; experience as a programming mentor.
- Ability and interest to work across cultures and geographies.
- Ability to complete statistical programming deliverables through the use of global outsource partner programming staff.
- Experience developing and managing a project plan using Microsoft Project or similar package.
- Active in professional societies.
- Experience in process improvement.
BARDS2020
eligibleforERP
SPjobs
VETJOBS
EBRG
Required Skills:
CDISC ADaM, Clinical Data Interchange Standards Consortium (CDISC) Standards, Clinical SAS Programming, Clinical Trials, Data Management, Data Modeling, Macro Programming, Numerical Analysis, Stakeholder Relationship Management, Waterfall ModelPreferred Skills:
Python (Programming Language), Regulatory Submissions, R ProgrammingCurrent 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.
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:
EEOC Know Your Rights
EEOC GINA Supplement
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
The salary range for this role is
$117,000.00 - $184,200.00This 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:
RegularRelocation:
DomesticVISA Sponsorship:
YesTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
10/23/2026*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.
Source: Merck & Co. on Workday · View original posting (opens in new tab)
Pay in context
This role's base floor ($117,000) is above 24% of the 979 Science & Research roles nationwide listed on this site; 12 others list the same floor. Their median floor is $140,000; the middle half runs from $117,000 to $169,320.
Only jobs on this site count, and each one publishes a base salary of $100,000 or more, so this compares six-figure jobs with each other, not with the whole market. Computed Nov 7, 2026.
This listingSenior Scientist Statistical Programming, Late-Stage (Hybrid)$117,000 to $184,200
Senior Scientist - Design Control (Hybrid)$117,000 to $184,200
Senior Scientist, Small Molecule Chemical Engineering$117,000 to $184,200
Senior Specialist, Process Automation$117,000 to $184,200
Sr. Specialist, Cybersecurity Engineering$117,000 to $184,200
Senior Scientist, Pharmacokinetics$117,000 to $184,200
Senior Scientist, DSCS Digital Technologies–Laboratory Automation, Automation Systems Engineer (Hybrid)$117,000 to $184,200
Chart as a table
| Role | Published base |
|---|---|
| Senior Scientist Statistical Programming, Late-Stage (Hybrid) (this listing) | $117,000 - $184,200 |
| Senior Scientist - Design Control (Hybrid) | $117,000 - $184,200 |
| Senior Scientist, Small Molecule Chemical Engineering | $117,000 - $184,200 |
| Senior Specialist, Process Automation | $117,000 - $184,200 |
| Sr. Specialist, Cybersecurity Engineering | $117,000 - $184,200 |
| Senior Scientist, Pharmacokinetics | $117,000 - $184,200 |
| Senior Scientist, DSCS Digital Technologies–Laboratory Automation, Automation Systems Engineer (Hybrid) | $117,000 - $184,200 |
Observed changes
- First observed on the employer's board
- Absent from the employer's board; confirmation pending
- Closure observed on Oct 23, 2026
- Reappeared on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-10-08
Where this pay comes from
Location as the employer wrote it: USA - Pennsylvania - North Wales (Upper Gwynedd) • USA - New Jersey - Rahway
$117,000.00 - $184,200.00
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
