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Promotional Review Committee Pharma Jobs (NOW HIRING)

Bausch & Lomb

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 ...

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Promotional Review Committee Pharma information

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$15

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$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.
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Promotional Review Committee Pharma jobs near you
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.

PRC (Promotional Review Committee) Coordinator

Inficare Technologies

Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

PRC (Promotional Review Committee) Coordinator - Onshore/Nearshore
Industry: Life Sciences / Pharma / Biotech
Work Model: Onshore (US) or Nearshore (LATAM / Canada support for US teams)
Role Overview
The PRC Coordinator manages the end-to-end promotional review process for marketing and medical materials, ensuring compliance with regulatory, legal, and brand standards. This role serves as the operational backbone of the PRC process, coordinating cross-functional stakeholders (Marketing, Medical, Legal, Regulatory) and optimizing review cycles.
Key Responsibilities
  • Coordinate and facilitate PRC review cycles for promotional and non-promotional materials (digital, print, HCP/patient-facing)
  • Manage submissions through systems such as Veeva PromoMats / Vault, Aprimo, or similar platforms
  • Schedule and lead PRC meetings, ensuring stakeholder alignment and timely reviews
  • Track material status, comments, approvals, and version control
  • Consolidate and reconcile cross-functional feedback into actionable updates for stakeholders
  • Ensure adherence to MLR compliance, FDA/OPDP guidelines, and internal SOPs
  • Maintain and report on KPIs (cycle time, approval timelines, review efficiency)
  • Identify process improvement opportunities for review cycle optimization
  • Support audits by maintaining accurate documentation and audit trails
  • Act as liaison between marketing teams and reviewers, ensuring clarity and efficiency

Required Qualifications
  • Bachelor's degree (Life Sciences, Business, Marketing, or related field)
  • 3-8 years of experience in:
    • PRC / MLR coordination
    • Marketing operations or regulatory support in pharma/biotech
  • Hands-on experience with Veeva Vault PromoMats (preferred) or similar tools
  • Strong understanding of promotional compliance and review workflows
  • Excellent organizational and project management skills
  • Ability to manage multiple deadlines in fast-paced environments
  • Strong communication and stakeholder management skills

Preferred Skills
  • Familiarity with US pharma regulatory environment (FDA, OPDP)
  • Experience supporting commercial launch or brand teams
  • Exposure to digital asset review and omnichannel campaigns
  • Data tracking/reporting via Excel, Power BI, or dashboards
  • Lean/Six Sigma or process improvement mindset

Onshore vs. Nearshore Expectations
Onshore (US-based):
  • Direct engagement with brand, medical, legal teams
  • Participation in live PRC discussions and decision-making forums
  • Greater ownership of stakeholder management and escalation handling

Nearshore (LATAM/Canada):
  • Operational execution of review coordination, tracking, and documentation
  • Time-zone aligned support for US teams
  • Increasing exposure to stakeholder interaction depending on seniority

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