Regulatory Affairs Associate III – PARC Operations

Teva Pharmaceuticals; West Chester (Chester County); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health Insurance

401(k) with employer match

Paid Time Off

Life and Disability Insurance

Employee Assistance Program

Tuition Assistance

Job summary

Teva Pharmaceuticals is seeking an Associate III, PARC Operations, to manage the Promotion and Advertising Review Committee (PARC) workflow, ensuring regulatory compliance and on-time submissions to FDA OPDP. The role coordinates PARC activities, tracks milestones, and maintains documentation across teams.

You will work with Teva’s regulatory and promotional teams to route materials, prepare agendas, review proofs, and generate reports on PARC metrics, while ensuring adherence to corporate

Qualifications

• 4–6 years of experience with review/approval of prescription drug advertising and promotion materials.
• Working knowledge of at least one electronic review system (Veeva) preferred.
• Familiarity with FDA 2253 submission process in eCTD format.
• Demonstrates excellent organization and follow-up skills.
• Ability to work independently within the PARC structure and with outside agencies.

Responsibilities

• Route review materials to assigned PARC team members within established timelines.
• Schedule and manage PARC meeting dates/times and issue PARC agendas promptly.
• Ensure all required activities leading up to PARC meetings are completed on time.
• Ensure PARC comments are addressed and understood by participants.
• Document final material changes and outcomes of PARC discussions.
• Review and approve proofs to incorporate PARC changes.
• Prepare and manage submissions to FDA OPDP within timelines.
• Proactively work with responsible functions to manage material expirations/renewals.
• Draft and review PARC process and internal guidance documents.
• Develop and run reports to support metrics and document compliance.

Skills

Attention to detail

Organizational skills

Independent worker

Team collaboration

Education

BA/BS Degree

Tools

Veeva

FDA 2253 submission process (eCTD)

Job description

Teva Pharmaceuticals is seeking an Associate III, PARC Operations, to manage the Promotion and Advertising Review Committee (PARC) workflow, ensuring regulatory compliance and on-time submissions to FDA OPDP. The role coordinates PARC activities, tracks milestones, and maintains documentation across teams.

You will work with Teva’s regulatory and promotional teams to route materials, prepare agendas, review proofs, and generate reports on PARC metrics, while ensuring adherence to corporate