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AbbVie

Global biopharmaceutical company developing medicines

Medical AQP Reviewer

Regulatory Compliance & EthicsConfirmed live in the last 24 hours
Full-timeMaidenhead, UKNo salary listed

About the Job

Requirements

  • A life science degree is essential.
  • At least 3 years of approvals experience with ABPI Code quality standards and up-to-date, detailed knowledge of the Code.
  • Experience understanding, analysing, and communicating complex pharmacy, pharmacology, and medical issues across different therapeutic areas.
  • Experience approving meetings in line with quality standards and the Code, including certification of overseas meetings.
  • Experience reviewing non-promotional materials, including corporate advertising, press releases, and market research material.
  • Demonstrated experience in reference checking and copy approval.

Responsibilities

  • Provide cross-therapy-area meeting approval support by examining UK meetings and certifying overseas meetings and travel arrangements.
  • Provide materials approval support by examining materials in line with company quality standards and the Code.
  • Attend Brand Team Meetings to ensure meeting plans and agendas are communicated and understood.
  • Attend ad-hoc brand team meetings and functional Medical meetings to support compliance with company approval standards.
  • Advise commercial and medical team project owners on compliant meeting planning.
  • Support continued implementation of a Code-compliant system for promotional and non-promotional activities throughout AbbVie and the marketplace, ensuring compliance with ABPI standards, the MHRA Blue Guide for advertising and promotion, applicable international codes of practice, and national codes and regulatory bodies.
  • Provide workable compliant solutions to support business development opportunities and product launches, and contribute to marketing campaign development.
  • Independently and promptly review and approve materials accurately in accordance with relevant codes of practice.
  • Evaluate materials during reviews, taking their risk profile into account when making decisions.
  • Provide guidance on UK Code requirements to global and overseas affiliates and the UK affiliate as needed.
  • Actively participate in cross-functional Medical Review Projects to build standard practices and solutions that meet business needs.
  • Support evaluation of materials exception reports and recommend corrective actions.
  • Adhere to the ABPI Code of Practice for the Pharmaceutical Industry in all aspects of work.
  • Present PMCPA Code cases to encourage team learning.
  • Serve as the subject-matter expert for meeting approvals and non-promotional materials, and as an expert resource for Brand teams.
  • Adhere to Medical Division standard operating procedures and guidelines.
  • Provide compliant solutions to meet business needs.
  • Comply with company policies and procedures to meet statutory, quality, and business requirements within AbbVie Ltd.'],
  • desirable [] are unspecified; no preferred qualifications are stated.
  • desirable

About the Company

AbbVie

Global biopharmaceutical company developing medicines

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company size
10,001+
Company stage
IPO
Headquarters
North Chicago, IL
Founded
1888

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