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Director, Data Management and Informatics

MSD


Job Location:

Rahway, NJ - USA

Yearly Salary: USD 173200 - 272600
Posted: 26 September 2026 (7 hours ago)
Application Deadline: 24 December 2026
Vacancies: 1 Vacancy

Job Summary

Job Description

We aspire to be the premier research-intensive biopharmaceutical company. At our company we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We use the power of leading-edge science to save and improve lives around the world. Join us in our mission to make a difference.


The Director will lead a business-critical organization responsible for regulatory data management informatics and analytics and enterprise data system business ownership. This role enables the delivery of trusted scientific and regulatory data across the product lifecycle -- from IND through NDA/BLA submissions post-filing activities product monitoring and inspection readiness while advancing scalable digital solutions that improve data accessibility automate manual processes strengthen compliance and enable data-driven decision-making. Partnering across Analytical Development Regulatory CMC Quality Digital our Research & Development Division and our Manufacturing Division organizations the Director will align business priorities deliver sustainable digital capabilities and build a high-performing team that accelerates scientific innovation and digital transformation


Responsibilities
  • Lead an integrated organization supporting regulatory data management informatics analytics and enterprise data system capabilities that enable scientific excellence regulatory compliance and digital transformation.
  • Deliver accurate traceable and submission-ready regulatory data across the product lifecycle (from IND NDA/BLA to post-approval filings).
  • Advance scalable analytics visualization and self-service data solutions that support proactive product monitoring operational transparency accelerate insights and support data-driven decisions.
  • Serve as business owner or representative for enterprise data systems driving strategy governance enhancements adoption and business value.
  • Translate scientific regulatory quality and business needs into scalable digital capabilities and data solutions that improve efficiency strengthen compliance and maximize the value of enterprise data assets.
  • Partner across scientific regulatory quality and technology organizations to deliver scalable sustainable and compliant solutions.
  • Drive standardization automation and continuous improvement to enhance data quality traceability and operational efficiency.
  • Ensure solutions are compliant inspection-ready scalable and aligned with enterprise data and digital strategies.

Qualifications

Required

  • Bachelors degree in Chemistry Pharmaceutical Sciences Biology Data Science Statistics Computer Science Engineering or related discipline with at least fifteen (15) years of analytical development chemistry pharmaceutical sciences informatics data science regulatory CMC Quality or a related experience; OR Masters degree with at least ten (10) years or Ph.D. with at least seven (7) years.
  • Proven leadership of data management informatics analytics laboratory systems enterprise data platforms or digital transformation initiatives in a regulated environment.
  • Strong people leadership stakeholder management and cross-functional influence skills with a track record of building high-performing teams and delivering business results.
  • Working knowledge of data integrity regulatory requirements quality systems laboratory operations and enterprise system lifecycle management.
  • Strong strategic thinking business acumen change leadership stakeholder engagement execution and problem-solving skills with a track record of delivering measurable business value through people processes data and technology.

Preferred

  • Experience in managing diverse teams of scientists contractors and cross-functional contributors.
  • Experience supporting regulatory submissions and post-filing activities from IND through NDA/BLA.
  • Experience applying analytical laboratory expertise to improve scientific data generation review and consumption across development stability quality and regulatory workflows.
  • Experience serving as a business owner or product owner for enterprise systems digital products or data capabilities.
  • Knowledge of AI/GenAI advanced analytics or emerging digital technologies and their application to scientific and regulatory data workflows.
  • Experience delivering trusted compliant and inspection-ready scientific and regulatory data that support development regulatory submissions and commercial products.
  • Demonstrated ability to develop scalable digital capabilities that improve data accessibility increase automation strengthen compliance and enable data-driven decisions.

Required Skills:

Academic Presentations Bioconjugation Computational Chemistry Creativity Data Analysis High-Throughput Experimentation (HTE) Organic Synthesis Professional Networking Project Leadership Research Proposal Development Scientific Leadership Scientific Literature Search Strategic Thinking Structure Based Drug Design Synthetic Chemistry

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.

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 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 anothers 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

$173200.00 - $272600.00

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 employees 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 can apply for this role through (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:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

10/9/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Director


About Company

Company Logo

Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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