Associate Principal Scientist Statistical Programming, Submission Data Standards Quality Management

Regulatory Toolkit; Pennsylvania; Hybrid; USD 142,000 - 224,000; Full time

Benefits offered by this job

401(k) plan

Annual bonus

Long-term incentive

Health insurance

Job summary

Merck is seeking an Associate Principal Statistical Programmer in the SDS QM area to oversee submission data standards quality management for global regulatory submissions. Responsibilities include planning, coaching teams, coordinating with vendors, and staying current with SDTM/ADaM standards to ensure high-quality deliverables.

The role requires leadership in regulatory submission deliverables, strong SDTM/ADaM expertise, and the ability to drive process improvements across departments and

Qualifications

• BA/BS in a relevant field plus 9+ years SAS programming experience in a clinical trial environment.
• MS in a relevant field plus 7+ years SAS programming experience in a clinical trial environment.

Responsibilities

• Oversee submission data standards planning and quality assurance for SDTM/ADaM deliverables.
• Coach project teams on regulatory submission preparation and SDTM mapping.
• Lead or participate in cross-functional regulatory submission activities with external partners.
• Maintain awareness of evolving industry data standards and ensure traceability of submissions.

Skills

SAS programming

CDISC SDTM

ADaM

Regulatory submissions

Define-XML

Education

BA/BS in a related field

MS in a related field

Tools

Pinnacle 21 Enterprise

Job description

Job Description

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our 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.

The Associate Principal Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards planning activities, coaching and consulting with project teams, outreach to external vendors and partners, and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.

The incumbent will be responsible for continuous improvement of our electronic submission process and providing tools and templates to support delivery focusing on traceability, quality assurance, data conformance and data fitness. The position is a key collaborator with statistical programming, statistics, regulatory and other project stakeholders and ensures 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.

Primary Activities

• PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes (CBER/CDER), attendance at meetings with regulatory agencies (FDA, EMA, PMDA).
• Guiding project teams preparing submission deliverables including use of Pinnacle 21 Enterprise.
• Up-versioning activities to specific versions of SDTM.
• Participation in industry teams and conferences on best practices.
• Membership on departmental strategic initiative project teams.

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

• Excellent interpersonal skills and ability to negotiate and collaborate effectively.
• Excellent written, oral, and presentation skills.
• Broad knowledge and significant experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings).
• Strong project management skills; leadership at a program level; determines approach and ensures consistency and directs development of others when opportunities arise; ability to engage key stakeholders.

Position Specific Required Skills and Experience

• US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development of electronic submission deliverables.
• Strong knowledge and practical experience with CDISC submission standards, including SDTM and ADaM, and associated submission deliverables such as Define-XML, SDRG, and ADRG.
• Strong working knowledge of SDTM standards, controlled terminology, and clinical data standardization, including application of standards across clinical studies and development programs.
• Experience providing technical guidance and leadership related to SDTM standards, data mapping, implementation, and issue resolution.
• Excels in technical writing, able to convert complex ideas and information into simple readable form.
• Strong project management and organizational skills, with the ability to manage multiple priorities, deliverables, dependencies, and stakeholders.
• Working knowledge of clinical data management and clinical development processes and their relationship to SDTM and downstream submission deliverables
• Demonstrated strategic thinking, with the ability to translate strategy into practical standards, processes, and implementation.
• Strong stakeholder management and collaboration skills, including the ability to anticipate stakeholder needs, build alignment, and work effectively across functions and geographies.

Preferred Skills and Experience

• Experience applying GenAI, automation, and advanced analytics technologies to improve standards development, implementation, and governance.
• Experience contributing to or leading Standards governance forums influencing cross-functional stakeholders and facilitating standards decisions, harmonization, and issue resolution.
• Experience with metadata repositories, standards libraries, mapping solutions, or related clinical standards technologies.
• Experience with process improvement, automation, and technology-enabled approaches to improve the efficiency, consistency, traceability, and scalability of standards implementation.
• Adaptable and resilient in a dynamic environment, effectively navigating change while quickly integrating into new projects, teams, and stakeholder groups.
• Ability and interest to work across cultures and geographies.
• Ability to complete statistical programming deliverables through the use of global outsource partner programming staff.
• Strong working knowledge of reporting processes (SOPs) and software development life cycle (SDLC).
• Experience developing and managing a project plan using Microsoft Project or similar package.
• Active in professional societies.
• Experience in process improvement.

Required Skills

• Business Process Creation
• Business Process Improvements
• Business Writing
• Change Management
• Data Management
• Data Modeling
• Global Coordination
• Influencing Skills
• Numerical Analysis
• Partner Relationship Management (PRM)
• Presentation Delivery
• Process Implementations
• Project Integration
• Project Leadership
• Project Management Leadership
• Stakeholder Management
• Stakeholder Relationship Management
• Standards Compliance
• Standards Development
• Statistical Programming
• Strategic Planning
• Strategic Thinking
• Strategy Development
• Waterfall Model

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.

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

Learn more about your rights, including under California, Colorado and other US State Acts

Salary Range

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.

Benefits

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

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

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

10/13/2026

*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.