Senior Director, Regulatory Affairs

Merck & Co.; North Wales (Montgomery County); Hybrid; USD 173,000 - 273,000; Full time

Job summary

Merck & Co., Inc. is seeking a Senior Director to oversee a team of promotional regulatory professionals responsible for US advertising and promotion review. The role drives regulatory strategy across multiple franchises and partners with commercial teams to align with FDA rules.

The position requires extensive experience in regulatory affairs, leadership, and cross-functional collaboration, with a focus on compliant promotional activities from development through market.

Qualifications

• Minimum 12 years' experience in pharmaceutical/biologics regulatory, clinical, medical, legal, and/or marketing disciplines, including advertising/promotional review work.
• Minimum 6 years' experience reviewing advertising and promotion materials or marketing programs for regulatory/legal compliance.
• Expert understanding of FDA regulations and company policies related to promotion development and implementation.

Responsibilities

• Leads a team of promotional regulatory reviewers to provide regulatory strategy across multiple therapeutic franchises for pipeline and in-line products.
• Partners with commercial and other stakeholders to develop a promotional regulatory strategy and product positioning that aligns with regulations.
• Serves as critical leadership point of contact for assigned brands and escalations, as needed.
• Oversees product labeling input, global regulatory strategy, and support of promotional messaging in clinical trial design and labeling.
• Interprets FDA perspectives and recommends policy or process changes as needed.
• Drives regulatory decisions with senior leadership and FDA.

Skills

Business Alignment

Cross-Functional Project Management

Decision Making

Global Regulatory Submissions

Goal Setting

Interpersonal Relationships

Negotiation

People Leadership

Policy Reviews

Policy Revisions

Regulatory Affairs Management

Regulatory Communications

Regulatory Compliance

Regulatory Documents

Regulatory Experience

Regulatory Management

Regulatory Processes

Regulatory Reporting

Regulatory Strategies

Regulatory Submissions

Stakeholder Negotiations

Strategic Planning

Strategic Thinking

Education

Bachelor's degree

Job description

Job Description

Senior Director manages a team of promotional regulatory professionals in the regulatory review of U.S. promotional materials for assigned products.

Summary of Responsibilities:

• Leads a team of promotional regulatory reviewers (senior specialists, associate directors, and individual contributor directors) to provide regulatory strategy across multiple therapeutic franchises for pipeline and in-line products that competitively positions our company's products, consistent with applicable FDA regulations and company policies for US advertising and promotion. Ensures strategy is aligned with overall corporate strategy and organizational goals.- The senior director will be responsible for providing a regulatory risk assessment and managing escalations with senior leaders.
• Partners with commercial and other stakeholders to develop a promotional regulatory strategy and product positioning that aligns commercial strategy with regulations. Drives optimal regulatory strategy, planning and delivery for advertising and promotion to support the overall business goals for therapeutic area(s) of focus.- Serves as critical leadership point of contact for assigned brands and associated escalations, as needed.-
• Serves as critical partner with HH, Legal and Medical on cross-divisional transformation work inclusive of process redesign and technology enablement.-
• Oversees direct report's product assignments and ensures collaboration and a cohesive and integrated regulatory strategy from early development through approval and marketing. Provides guidance and coaching to direct reports on their input to product labeling, global regulatory team strategy, adequate support of promotional messaging and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the use of study results in U.S. promotion. Ensures direct reports are compliant with corporate policies and complete all required corporate and compliance training.
• Demonstrated ability to impact and drive regulatory decisions with senior company leadership and with FDA.- Helps shape regulatory policy with OPDP and APLB on emerging topics and innovative technologies.-- Serves on external promotional regulatory planning committees and contributes to our company's regulatory leadership by presenting at leading external regulatory meetings (DIA, FDLI, RAPS etc.).
• Identifies the need for development, refinement, and implementation of department and corporate strategic initiatives that drive effective, compliant promotional regulatory review.-
• Analyzes business needs and capacity and contributes to staffing discussions with Executive Director.
• Serves as a liaison with OPDP and/or APLB Team Leaders or reviewers for business-critical initiatives.
• Effectively interprets and communicates FDA perspectives to relevant company stakeholders and recommends policy and/or process changes as needed.

Education Minimum Requirement:

• Bachelor of Arts or Science Degree, with advanced degree preferred.- Strongly preferred to have a science-related degree such as biology, chemistry, nursing, pharmacy, social sciences, or QA/regulatory affairs.

Required Experience and Skills:

• Minimum 12 years' experience in pharmaceutical/biologics regulatory, clinical, medical, legal, and or marketing disciplines, including demonstrated advertising/promotional review work
• Minimum 6 years' experience reviewing advertising and promotion materials or marketing programs for regulatory/legal compliance
• Expert understanding and application of FDA regulations and our company's policies and procedures related to promotion development and implementation and promotion review processes
• Expert understanding of the clinical development process, including labeling development and FDA approval processes
• Demonstrated ability to lead and direct complex activities of a Team and drive work effectively in a cross-functional team environment
• Collaborative - ability to build deep relationships cross-functionally to drive optimal performance
• Demonstrated superior verbal and written communication skills
• Strong interpersonal and negotiation skills with ability to demonstrate strategic and analytic thinking
• Demonstrated ability to negotiate and influence others effectively
• Proven track record of effective collaboration with external stakeholders which may include FDA branches (OPDP, APLB), alliance relationships with peer companies as well as external consortia and trade organizations such as DIA.- Strong judgment and decision-making skills.-----

Required Skills:

Business Alignment, Cross-Functional Project Management, Decision Making, Global Regulatory Submissions, Goal Setting, Interpersonal Relationships, Negotiation, People Leadership, Policy Reviews, Policy Revisions, Regulatory Affairs Management, Regulatory Communications, Regulatory Compliance, Regulatory Documents, Regulatory Experience, Regulatory Management, Regulatory Processes, Regulatory Reporting, Regulatory Strategies, Regulatory Submissions, Stakeholder Negotiations, Strategic Planning, Strategic Thinking

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:

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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

$173,200.00 - $272,600.00

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 .

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:

No relocation

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:

10/2/2026

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.

Requisition ID:

R418196