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- Tasks: Lead medical affairs for innovative medical devices and support new product launches.
- Company: Global leader in the medical device industry with a focus on innovation.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by shaping medical strategies and collaborating globally.
- Qualifications: Medical degree and 5 years of clinical experience required.
- Other info: Join a dynamic team and enjoy occasional travel to conferences.
The predicted salary is between 72000 - 108000 £ per year.
A global organisation operating within a highly regulated medical device environment is seeking a Medical Associate Director to support medical affairs activities across a broad and diverse product portfolio. This role plays a critical part in new product introductions, clinical evaluation, safety oversight, and cross-functional decision-making, working closely with Quality, Regulatory, and global Medical Affairs stakeholders. It is well suited to a clinically trained professional looking to apply medical judgement in a strategic, international setting.
Responsibilities
- Provide medical input to support new product introductions and front-end innovation initiatives
- Contribute to the design of clinical trials, including endpoint definition
- Review Clinical Evaluation Reports (CERs) for medical accuracy and clinical relevance
- Partner with regulatory leads to ensure alignment with regulatory expectations
- Review publications to ensure on-label compliance and appropriate medical positioning
- Review marketing and sales materials for medical accuracy and claim substantiation
- Participate in safety boards, providing medical health and safety assessments
- Support health evaluations across a large global manufacturing and product footprint
- Act as the medical affairs voice within cross-functional project teams
- Collaborate closely with Quality, Regulatory, Medical Writing, and Commercial teams
- Provide medical input into product risk assessments and issue resolution
- Attend conferences to build hands-on product and clinical understanding
- Work effectively with US-based stakeholders, requiring occasional evening flexibility
- Gradually transition from shadowing into independent ownership of medical affairs activities
About You
- Medical degree (MD or equivalent)
- Minimum 5 years’ clinical experience with direct patient interaction
- Experience or exposure to medical devices strongly preferred
- Understanding of clinical trials and clinical evaluation processes
- Strong ability to lead and influence cross-functional teams
- Excellent written and verbal communication skills
- Willingness to travel occasionally and work flexibly with global teams
Medical Associate Director in London employer: Consult
Contact Detail:
Consult Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Associate Director in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical field, especially those who work with medical devices. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your clinical knowledge and understanding of regulatory processes. We recommend practising common interview questions related to medical affairs to showcase your expertise.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds.
✨Tip Number 4
Apply through our website for the best chance at landing that Medical Associate Director role. We’re always on the lookout for passionate candidates who want to make a difference in medical affairs!
We think you need these skills to ace Medical Associate Director in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the Medical Associate Director role. Highlight your clinical experience and any work with medical devices to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this position, focusing on your medical judgement and strategic thinking in a global context.
Showcase Your Communication Skills: Since excellent written communication is key for this role, ensure your application is clear, concise, and free of jargon. We want to see how you can convey complex medical information effectively!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role without any hiccups!
How to prepare for a job interview at Consult
✨Know Your Medical Stuff
Make sure you brush up on your medical knowledge, especially around clinical trials and medical devices. Be ready to discuss how your clinical experience can directly contribute to the role, as they’ll want to see that you can apply your medical judgement effectively.
✨Understand the Company’s Products
Take some time to research the company’s product portfolio. Familiarise yourself with their latest innovations and any recent publications. This will not only show your interest but also help you articulate how you can support new product introductions.
✨Prepare for Cross-Functional Collaboration
Since this role involves working closely with various teams like Quality and Regulatory, think of examples from your past experiences where you successfully collaborated across functions. Be ready to share how you can influence and lead these teams towards common goals.
✨Showcase Your Communication Skills
As communication is key in this role, practice articulating your thoughts clearly and concisely. Prepare to discuss how you’ve effectively communicated complex medical information in the past, whether it’s through reports, presentations, or discussions with stakeholders.
