1

Promotional Review Committee Pharma Jobs (NOW HIRING)

OR

$149K - $197K/yr

Manages the Regulatory Promotional reviewers for products who represent Regulatory Affairs on the promotional review committee for preapproval and marketed products. This position may require ...

Reg Affairs Director

$153K - $202K/yr

Lead review and approval of promotional materials through the Medical, Legal and Regulatory review committee (MLR). * Ensure materials are accurate, balanced, and supported by substantial evidence.

Lead review and approval of promotional materials through the Medical, Legal and Regulatory review committee (MLR). * Ensure materials are accurate, balanced, and supported by substantial evidence.

NC · On-site

Promotional Review Committee * Manage submissions and represent Patient Services at the cross-departmental Promotional Review Committee for two to four BIIB products. * Partner with medical, legal ...

OR · On-site

ARS Pharma is committed to improving patients' lives and building healthier communities. We foster ... the Promotional Review Committee, and ensure Medical Affairs activities are conducted with ...

Showing results 21-40

Promotional Review Committee Pharma information

See salary details

$15

$25

$33

How much do promotional review committee pharma jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for promotional review committee pharma in the United States is $25.85, according to ZipRecruiter salary data. Most workers in this role earn between $21.39 and $30.53 per hour, depending on experience, location, and employer.

What are some common challenges faced by members of a Promotional Review Committee in pharma?

Members of a Promotional Review Committee (PRC) in pharma often encounter challenges related to balancing regulatory compliance with effective marketing strategies. Ensuring that promotional materials adhere to strict FDA and other global guidelines while also meeting business objectives requires careful review and collaboration between regulatory, legal, medical, and marketing teams. Tight deadlines and frequent updates to regulations can add to the complexity, making clear communication and attention to detail essential skills for success in this role.

What is a Promotional Review Committee in pharma?

A Promotional Review Committee (PRC) in the pharmaceutical industry is a cross-functional team responsible for reviewing and approving promotional materials and communications to ensure they comply with regulatory, legal, and company standards. The committee typically includes representatives from medical, legal, regulatory, and marketing departments. Their primary role is to assess whether promotional content is accurate, balanced, and not misleading, and that it adheres to FDA and other relevant guidelines. PRC meetings are essential to ensure patient safety, maintain company reputation, and avoid regulatory penalties. The committee's work helps ensure that all promotional activities are ethical and compliant.

What is the difference between Promotional Review Committee Pharma vs Medical Affairs Specialist?

AspectPromotional Review Committee PharmaMedical Affairs Specialist
Primary RoleReview and approve promotional materials for compliance with regulationsProvide scientific and medical support, develop medical strategies
Required CredentialsPharmacy, medical, or regulatory background often preferredMedical degree or related scientific qualification
Work EnvironmentCross-functional teams, compliance departments, regulatory agenciesMedical departments, research teams, field medical teams

While both roles require scientific knowledge and regulatory understanding, the Promotional Review Committee Pharma focuses on reviewing promotional content for compliance, whereas the Medical Affairs Specialist provides scientific support and medical insights to the organization.

What are the key skills and qualifications needed to thrive as a member of a Promotional Review Committee in pharma?

To thrive as a member of a Promotional Review Committee in Pharma, you need a solid understanding of pharmaceutical regulations, clinical data, and medical writing, typically supported by a degree in life sciences or pharmacy. Familiarity with regulatory guidelines (such as FDA or EMA), document management systems, and promotional review platforms is essential. Strong attention to detail, effective collaboration, and clear communication are vital soft skills in this multidisciplinary environment. These skills ensure that promotional materials are accurate, compliant, and ethically sound, protecting both patient safety and company reputation.
More about Promotional Review Committee Pharma jobs
What cities are hiring for Promotional Review Committee Pharma jobs? Cities with the most Promotional Review Committee Pharma job openings:
What states have the most Promotional Review Committee Pharma jobs? States with the most job openings for Promotional Review Committee Pharma jobs include:
Infographic showing various Promotional Review Committee Pharma job openings in the United States as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $53,769 per year, or $25.9 per hour.

Senior Director, Regulatory Affairs (Ad Promo) (15511)

Bausch & Lomb

OR

$149K - $197K/yr

Other

Medical, Dental, Vision, Life, Retirement

Posted 27 days ago


Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

23rd of 536 rated manufacturers


Job description

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it-where your skills and values drive our collective progress and impact.

The Senior Director of Advertising & Promotion- Regulatory Affairs drug and device products manages and, if required participates in, the reviews and approvals of advertising and promotional labeling pieces for prescription, over the counter, and cosmetics products for primarily the US but also supports Canada. The Senior Director is responsible for ensuring the pieces are in compliance with regulatory agencies requirements.

Responsibilities:

  • Manages the Regulatory Promotional reviewers for products who represent Regulatory Affairs on the promotional review committee for preapproval and marketed products. This position may require reviewing promotional materials if the company requires it and escalations. This person is responsible for compliance with regulatory requirements while meeting Company's strategic promotional objectives.
  • Provide guidance on proposed claims for products in development and development of ISI and brief summaries.
  • Regularly monitor the regulatory compliance trends in industry, interpret new regulations, guidance documents and enforcement letters.
  • Update the Regulatory Ad Promo staff, review committees and appropriate other company staff regarding changes in the current regulatory environment at FDA's Office of Prescription Drug Promotion (OPDP), Canada Pharmaceutical Advertising Advisory Board (PAAB) and other regulatory considerations that may impact business. Develop or revise procedures needed.
  • Review packages for regulatory advice, resolution of FDA and Canadian action letters and leads the company in discussions with the FDA OPDP and Canada PAAB.
  • Coordinate companywide ongoing regulatory training on regulatory issues pertaining to promotion of Company products.
  • Represents regulatory affairs in cross functional prescription product promotional review teams as required, participate in development committees for processes and procedures relating to ad promo.
  • Interacts with Legal, Compliance and Medical Affairs regularly. Also works with Quality related to internal audits and CAPAs, as needed.

Qualifications:

  • Bachelor's degree in science or health related discipline required (Advanced degree PhD, MD, MS, PharmD preferred). Minimum 10 years of regulatory affairs product advertising and promotion and people management experience required. GI experience - preferred.
  • Broad knowledge of the pharmaceutical industry.
  • Demonstrated ability to contribute to a continuous learning and process improvement environment.
  • Detail-oriented with the ability to promptly assess documents for accuracy as well as consistency.
  • Strong interpersonal skills with the ability to influence others in a positive and effective manner.
  • Ability to work in a team environment.
  • Working knowledge of pharmaceutical and device development and approval process.
  • Excellent communication skills; both oral and written.

The range of starting base pay for this role is 215K - 296K.  Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan.

Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, stock purchase plan, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts.

We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.


What Bausch & Lomb employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Bausch & Lomb logo

About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853