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For Companies At a Glance
- Tasks: Lead medical strategy and oversee clinical activities for innovative healthcare products.
- Company: Global leader in medical devices with a focus on innovation and quality.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by guiding cutting-edge medical technologies.
- Qualifications: MD or equivalent, 5+ years clinical experience, and strong communication skills.
- Other info: Collaborative environment with opportunities to engage with top clinicians globally.
The predicted salary is between 36000 - 60000 £ per year.
Location: Remote (UK-based)
Travel: Up to 25% (UK & international)
Our client is a leading global medical device manufacturer with a strong track record of developing and commercialising innovative healthcare technologies. The organisation brings together clinical insight, engineering excellence, and data-driven approaches to deliver high-quality medical solutions used by healthcare professionals globally.
Role Overview
The Associate Medical Director will play a key role in providing medical leadership and clinical oversight across the full product lifecycle. This position works in close partnership with internal stakeholders to support clinical strategy, product development, regulatory submissions, and post-market activities. The role is inherently cross-functional, requiring collaboration with R&D, Quality, Regulatory Affairs, and Commercial teams, as well as engagement with external clinicians and Key Opinion Leaders to support evidence generation and medical strategy.
Key Responsibilities
- Provide medical expertise and clinical guidance to product development activities, risk management, and customer-facing discussions
- Support the planning, conduct, and interpretation of clinical studies, including both pre-market and post-market investigations
- Act as medical monitor for clinical trials, reviewing safety data, evaluating adverse events, and ensuring appropriate patient protection
- Contribute medical input to post-market surveillance and complaint investigations
- Work closely with Regulatory Affairs and Quality teams to ensure compliance with applicable medical device regulations and clinical standards
- Build and maintain effective relationships with external clinical experts, investigators, and Key Opinion Leaders
- Support the creation and review of medical, scientific, and training materials
- Provide medical input to internal training initiatives and broader medical affairs strategies
Skills & Experience
- MD, MBBS, or equivalent recognised medical degree (active medical registration preferred)
- At least 5 years of post-qualification clinical experience
- Previous Medical Doctor
- Demonstrated experience within the medical device industry, ideally in a medical affairs, clinical research, or medical monitoring capacity
- Strong understanding of clinical research processes, GCP, safety reporting, and medical device regulatory frameworks
- Proven ability to influence and collaborate within matrixed, cross-functional environments
- Excellent written and verbal communication skills, with the ability to explain complex medical concepts clearly
- Analytical mindset with strong clinical judgement and problem-solving capability
- Comfortable working in a dynamic, fast-paced environment
- Postgraduate qualifications in medicine, management, or a related discipline
- Prior experience supporting regulatory interactions or clinical submissions
Associate Medical Director in Slough employer: ECS
Contact Detail:
ECS Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Medical Director in Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical device industry and let them know you're on the hunt for an Associate Medical Director role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews by brushing up on your clinical knowledge and understanding of the product lifecycle. Be ready to discuss how your experience aligns with the responsibilities outlined in the job description, especially around clinical studies and regulatory compliance.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that resonate with your values and expertise. Use our website to find roles that match your skills and interests, and tailor your approach to each application to stand out from the crowd.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show your genuine interest in the role and the company.
We think you need these skills to ace Associate Medical Director in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience mentioned in the job description. Highlight your medical expertise, clinical oversight experience, and any relevant work in the medical device industry. We want to see how you fit into our world!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background aligns with our needs. Don’t forget to mention your collaborative spirit and ability to work cross-functionally, as that’s key for us.
Showcase Your Communication Skills: Since excellent communication is crucial for this role, make sure your application showcases your ability to explain complex medical concepts clearly. Whether it's in your CV or cover letter, we want to see your knack for clear and concise writing.
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. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at ECS
✨Know Your Medical Stuff
Make sure you brush up on your medical knowledge, especially around clinical research processes and medical device regulations. Be ready to discuss your experience in these areas and how it relates to the role.
✨Showcase Your Collaboration Skills
This role is all about working with different teams, so be prepared to share examples of how you've successfully collaborated in the past. Highlight any experiences where you’ve worked with R&D, Quality, or Regulatory Affairs.
✨Prepare for Clinical Scenarios
Think about potential clinical scenarios you might face in this role. Be ready to discuss how you would approach clinical studies, safety data evaluation, and patient protection. This will show your analytical mindset and problem-solving skills.
✨Communicate Clearly
Practice explaining complex medical concepts in simple terms. You’ll need to demonstrate excellent communication skills, so consider how you can convey your ideas clearly and effectively during the interview.
