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- Tasks: Support the Medical Director and shape medical strategies for rare diseases.
- Company: Join a leading pharmaceutical organisation making a difference in healthcare.
- Benefits: Enjoy a fixed-term contract with opportunities for professional growth and networking.
- Why this job: Be a key player in impactful medical affairs and collaborate with diverse teams.
- Qualifications: A scientific degree and prior Medical Affairs experience in the pharmaceutical industry are essential.
- Other info: Engage with healthcare professionals and contribute to clinical research initiatives.
The predicted salary is between 43200 - 72000 £ per year.
A leading pharmaceutical organisation is looking for a Medical Affairs Advisor to join its European medical team. Supporting the Medical Director, this person will act as a key conduit between the external healthcare environment and internal business functions. This position will play a critical role in shaping and implementing the medical strategy for both marketed products and pipeline assets, while ensuring alignment across cross-functional teams. The successful candidate will serve as a trusted source of scientific and clinical expertise for internal and external stakeholders.
Key Responsibilities
- Act as a strategic medical partner within cross-functional brand teams, providing scientific insights and shaping the direction of assets in Rare Diseases.
- Develop and maintain strong relationships with external stakeholders including healthcare professionals, payers, policy makers, and patient advocacy groups.
- Contribute to the creation and execution of the annual Regional Medical Plan, ensuring alignment with global strategies and objectives.
- Attend medical events, congresses, symposia and advisory boards.
- Liaising with external vendors (such as medical communications agencies).
- Collaborate with the European Regulatory Affairs, Market Access, Pharmacovigilance, and Health Outcomes teams to support integrated regional activities.
- Review and approve medical materials, ensuring compliance with industry codes and regulations.
- Respond to scientific inquiries from healthcare professionals, providing high-quality and timely data and insights.
- Support evidence generation planning, clinical research initiatives, and publication development in alignment with market needs.
- Assist in the feasibility and execution of clinical trials, including site selection and engagement with external experts.
- Uphold regulatory, ethical, and corporate compliance standards.
Required Qualifications and Experience
- A scientific or clinical degree (e.g., BSc, MSc, PhD, PharmD, MD) is essential.
- Prior experience in a Medical Affairs role within the pharmaceutical industry at a European level is required.
- Strong understanding of the European healthcare environment and clinical practices.
- In-depth knowledge of pharmaceutical industry codes of practice (e.g., ABPI, EFPIA, IFPMA).
- Demonstrated ability to work cross-functionally, manage multiple priorities, and operate in a results-driven setting.
- Rare Diseases expertise is preferred but not essential.
Medical Advisor employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Advisor
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in Medical Affairs. Attend relevant conferences and events to meet potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in the European healthcare environment. This knowledge will not only help you in interviews but also demonstrate your commitment to staying informed in this rapidly evolving field.
✨Tip Number 3
Engage with patient advocacy groups and healthcare professionals to understand their perspectives on Rare Diseases. This insight can be invaluable when discussing strategies and building relationships in your future role.
✨Tip Number 4
Prepare to discuss specific examples of how you've successfully collaborated with cross-functional teams in the past. Highlighting your ability to manage multiple priorities and drive results will set you apart from other candidates.
We think you need these skills to ace Medical Advisor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Medical Affairs, particularly within the pharmaceutical industry. Emphasise any roles that involved cross-functional collaboration or strategic medical partnerships.
Craft a Compelling Cover Letter: In your cover letter, express your passion for Rare Diseases and how your background aligns with the company's goals. Mention specific experiences that demonstrate your ability to develop relationships with healthcare professionals and stakeholders.
Highlight Relevant Qualifications: Clearly state your scientific or clinical degree and any additional qualifications. If you have experience with European healthcare regulations or industry codes, make sure to include that as well.
Showcase Your Soft Skills: In addition to technical expertise, highlight your soft skills such as communication, teamwork, and adaptability. These are crucial for a role that requires liaising with various stakeholders and managing multiple priorities.
How to prepare for a job interview at Meet Life Sciences
✨Know Your Medical Affairs
Make sure you have a solid understanding of the role of a Medical Affairs Advisor, especially in the context of Rare Diseases. Familiarise yourself with the latest trends and challenges in the European healthcare environment to demonstrate your expertise.
✨Build Relationships
Highlight your ability to develop strong relationships with external stakeholders. Be prepared to discuss examples of how you've successfully collaborated with healthcare professionals, payers, and policy makers in previous roles.
✨Showcase Your Strategic Thinking
Prepare to discuss how you can contribute to the creation and execution of a Regional Medical Plan. Think about how you would align local strategies with global objectives and be ready to share your insights on this process.
✨Understand Compliance Standards
Familiarise yourself with industry codes of practice such as ABPI and EFPIA. Be ready to discuss how you ensure compliance in your work, particularly when reviewing medical materials or responding to scientific inquiries.
