Associate Principal Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)

Merck (MSD)
Location
USA - Pennsylvania - North Wales (Upper Gwynedd)
Job Type
Full-time
Posted
September 11, 2026
Views
7
Salary Range
$142k - $224k USD

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 leads the statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development 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 9 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 7 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)
  • Leads large and/or complex projects, effectively balances competing priorities, and collaborates closely with key stakeholders to achieve project objectives

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
  • US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables
  • 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

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 leads the statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development 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 9 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 7 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)
  • Leads large and/or complex projects, effectively balances competing priorities, and collaborates closely with key stakeholders to achieve project objectives

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
  • US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables
  • 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., Python, R, R Shiny, Claude, etc.)
  • Demonstrated success in the assurance of deliverable quality and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life cycle (SDLC)
  • 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

Base SAS, Clinical Development, Data Management, Data Modeling, FDA Submissions, Influencing Skills, Oncology, Presentation Delivery, Process Improvements, Project Management, Project Planning, Resource Planning, Stakeholder Management, Statistical Programming, Strategic Planning, Strategic Thinking

Preferred Skills

Artificial Intelligence (AI), Generative AI, Python (Programming Language), R Programming

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.

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

$142,400.00 - $224,100.00

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

Domestic

VISA Sponsorship

Yes

Travel Requirements

10%

Flexible Work Arrangements

Hybrid

Shift

Not Indicated

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

10/10/2026*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.

Researching Merck (MSD) before you apply?

See 31 open roles · Verified H-1B salary data · Clinical-trial hiring momentum · Culture, benefits & locations.

View Merck (MSD) profile

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The position is located in North Wales (Upper Gwynedd), Pennsylvania, USA, and operates under a hybrid work arrangement.
What are the required qualifications and experience levels for this role?
You need a BA/BS degree with at least 9 years of SAS programming experience in a clinical trial environment, or an MS degree with at least 7 years of the same experience. Significant expertise in SAS, clinical trial programming, CDISC/ADaM standards, and US/worldwide drug or vaccine regulatory submissions is required.
What are the key responsibilities of this position?
You will lead statistical programming activities for late-stage clinical development projects, develop and validate analysis and reporting deliverables, design and maintain statistical datasets, manage project plans and resource forecasting, and coordinate a global programming team that includes outsource provider staff.
What is the salary range for this role?
The salary range is $142,400.00 to $224,100.00. The successful candidate will also be eligible for an annual bonus and long-term incentives, if applicable.
Are visa sponsorship and relocation support offered for this position?
Yes, visa sponsorship is available for this position, and domestic relocation support is also offered.
What benefits does the company provide?
Benefits include medical, dental, and vision healthcare, other insurance benefits for employees and families, retirement benefits including a 401(k), paid holidays, vacation, and compassionate and sick days.
What is the application deadline and how do I apply?
You can apply online at https://jobs.merck.com/us/en. The application deadline is October 10, 2026, and you must submit your application no later than 11:59:59 PM on October 9, 2026.

Ready to Apply?

Apply for this Position

You'll be redirected to the company's application page

Share this job:

Explore Merck (MSD)

Research the company before you apply.

  • 31 open roles
  • Verified H-1B salary data
  • Clinical-trial hiring momentum
  • Culture, benefits & locations
View company profile

Job Information

Source: manual
AI Relevance: 92/100 (Highly relevant)
Remote Type: onsite
Allowed Locations: Worldwide
Skills & Tags:
merck (msd) artificial intelligence biostatistics oncology clinical

Get Similar Jobs by Email

Weekly digest of Merck (MSD) and similar companies. Free.

Related Jobs

Apply for this Position

Get weekly job alerts