MD Job Opportunity at AbbVie – Medical Advisor Role in the UK
AbbVie is offering an exciting MD job opportunity for the position of Medical Advisor in Maidenhead, UK. This full-time role within Research & Development is ideal for qualified medical professionals seeking to advance their careers through AbbVie careers, contributing to medical affairs, clinical research, and patient safety in one of the leading pharmaceutical jobs in the UK.
Job Details:
- Job Position: Medical Advisor
- Location: Maidenhead, United Kingdom
- Job ID: R00137606
About the Company:
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. Through AbbVie careers, the company strives to make a remarkable impact on people’s lives across immunology, oncology, neuroscience, and eye care, making it a preferred choice for medical professionals exploring jobs in the UK.
Qualifications:
- Medical Doctorate (M.D.) degree or equivalent required.
- Residency and/or fellowship completion preferred.
- Minimum of 2 years of experience in clinical trials or medical affairs.
- Strong knowledge of clinical trial methodology and regulatory requirements.
- Expertise in a relevant therapeutic specialty.
- Excellent oral and written English communication skills.
- Multilingual skills preferred for multi-country responsibilities.
MD Job Description:
This MD job provides specialist medical and scientific strategic input for one or a cluster of countries within Western Europe & Canada. The role supports core medical affairs activities such as healthcare professional interactions, clinical and scientific data generation, medical education initiatives, and patient safety monitoring.
The Medical Advisor works closely with sales, marketing, and commercial teams to provide strategic medical input into brand strategies, promotional material generation, product launches, and market access initiatives within AbbVie careers.
MD Job – Key Responsibilities:
- Provide leadership, oversight, and support for assigned products and projects.
- Establish and approve scientific methods for hypotheses, rationale, and protocol design.
- Participate in clinical trial safety, product safety, and risk management plans.
- Oversee clinical trials and resolve safety-related issues, including AEs and SAEs.
- Initiate medical affairs activities supporting the overall product, scientific, and business strategy.
- Deliver scientific and medical education to investigators and global project teams.
- Ensure compliance with regulatory requirements governing clinical studies.
- Lead research initiatives resulting in high-quality publications, supporting AbbVie’s presence in the UK.
