Clinical Development Medical Director - EMEA / UK
Clinical Development Medical Director - EMEA / UK

Clinical Development Medical Director - EMEA / UK

Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical development and medical strategies for innovative autoimmune therapies.
  • Company: Join a pioneering biopharmaceutical company focused on severe autoimmune diseases.
  • Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
  • Why this job: Make a real difference in patients' lives with cutting-edge therapies.
  • Qualifications: MD or equivalent, 5-8 years in biopharma, experience in rare diseases preferred.
  • Other info: Dynamic role with cross-functional collaboration and significant impact on clinical outcomes.

The predicted salary is between 72000 - 108000 £ per year.

About Us

We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology – enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation – enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections.

About the Role

We are seeking a dynamic and scientifically driven Clinical Development Medical Director to join our Medical Affairs team. Reporting to our Executive Medical Affairs Director, EMEA/UK Lead, this cross-functional role bridges clinical development and medical affairs, providing scientific and clinical leadership to support the advancement of our pipeline and the execution of medical strategies. The ideal candidate will bring strong clinical acumen, experience in rare diseases and/or autoimmunology, and a collaborative mindset to help drive impactful medical and scientific initiatives. Day to day you will support clinical trial executions and enrollment through strong Principal Investigator relationship building. This is an exciting opportunity to join a late-stage clinical company with a pipeline of potential best in class autoimmune therapies. We are building a culture of individuals who hold our core principles at the center of our operations, with the goal to elevate the care of our patients’ lives. We are open to you working remotely. You must be located in the United Kingdom.

Key Responsibilities

  • Scientific & Clinical Leadership: Serve as a subject matter expert on the company’s pipeline assets, providing deep clinical and scientific insights. Support the development and execution of global medical affairs strategies, including evidence generation, scientific communications, and external engagement.
  • Medical Affairs Support: Contribute to the development of medical education materials, scientific publications, and congress presentations. Collaborate with Medical Science Liaisons (MSLs) to ensure scientific alignment and support field medical activities. Participate in the planning and execution of advisory boards and KOL engagement initiatives.
  • Clinical Development Interface: Act as a key liaison between Medical Affairs and Clinical Development, ensuring alignment on clinical trial design, data interpretation, and lifecycle planning. Provide medical input into clinical protocols, investigator brochures, and regulatory documents as needed.
  • Evidence Generation: Support the design and execution of investigator-initiated studies (IIS), real-world evidence (RWE) programs, and post-marketing studies. Collaborate with cross-functional teams to identify data gaps and develop strategies to address them.
  • Cross-Functional Collaboration: Work closely with Regulatory, Commercial, Market Access, and other internal stakeholders to ensure scientific consistency and strategic alignment. Contribute to launch readiness and lifecycle management planning.

Experience

  • MD, DO, or equivalent medical degree required; board certification in a relevant specialty preferred.
  • Minimum 5–8 years of experience in the biopharmaceutical industry, with at least 3 years in a medical affairs or clinical development role.
  • Experience in rare diseases and/or autoimmunology strongly preferred.
  • Proven ability to interpret and communicate complex clinical data to diverse audiences.
  • Strong interpersonal and communication skills, with a collaborative and proactive approach.
  • Ability to thrive in a fast-paced, evolving environment with a high degree of autonomy.
  • Ability to travel up to 50% including to company events, potential relevant conferences and clinically relevant trial sites.

Clinical Development Medical Director - EMEA / UK employer: Dianthus Therapeutics, Inc.

At our company, we are dedicated to developing innovative therapies for patients with severe autoimmune diseases, fostering a collaborative and dynamic work environment that prioritises scientific excellence and patient care. As a Clinical Development Medical Director, you will have the opportunity to lead impactful medical initiatives while enjoying the flexibility of remote work within the UK, alongside robust professional growth opportunities in a late-stage clinical setting. Join us in our mission to elevate patient lives through cutting-edge science and a supportive culture that values your contributions.
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Contact Detail:

Dianthus Therapeutics, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Development Medical Director - EMEA / UK

✨Network Like a Pro

Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to clinical development and autoimmune diseases. Building relationships can open doors to opportunities that aren’t even advertised.

✨Showcase Your Expertise

When you get the chance to chat with potential employers, don’t hold back on sharing your knowledge. Discuss your experience with clinical trials and rare diseases confidently. We want to see your passion and expertise shine through!

✨Follow Up After Interviews

After an interview, drop a quick thank-you email to express your appreciation for the opportunity. It’s a simple gesture that keeps you fresh in their minds and shows your enthusiasm for the role.

✨Apply Through Our Website

Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Dianthus Therapeutics.

We think you need these skills to ace Clinical Development Medical Director - EMEA / UK

Clinical Acumen
Experience in Rare Diseases
Experience in Autoimmunology
Scientific Leadership
Medical Affairs Strategy Development
Evidence Generation
Clinical Trial Design
Data Interpretation
Regulatory Knowledge
Interpersonal Skills
Communication Skills
Collaboration
Proactive Approach
Ability to Work Autonomously
Adaptability in Fast-Paced Environments

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of Clinical Development Medical Director. Highlight your experience in rare diseases and autoimmunology, and don’t forget to showcase your clinical acumen and leadership skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about our mission at StudySmarter and how your background aligns with the responsibilities of the role. Be genuine and let your personality come through.

Showcase Your Collaborative Spirit: We value collaboration, so make sure to highlight any cross-functional projects you've worked on. Share examples of how you’ve built relationships with Principal Investigators or other stakeholders in your previous roles.

Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to see what you bring to the table!

How to prepare for a job interview at Dianthus Therapeutics, Inc.

✨Know Your Stuff

Make sure you have a solid understanding of the company’s pipeline assets and the science behind them. Brush up on the specifics of claseprubart and DNTH212, as well as their mechanisms of action. This will not only show your expertise but also your genuine interest in the role.

✨Showcase Your Experience

Prepare to discuss your previous experience in medical affairs or clinical development, especially in rare diseases and autoimmunology. Have specific examples ready that highlight your leadership skills and how you've successfully collaborated with cross-functional teams.

✨Engage with Questions

Don’t just wait for questions to be thrown at you; come prepared with insightful questions about the company’s strategies and future directions. This demonstrates your proactive mindset and helps you gauge if the company culture aligns with your values.

✨Be Ready for Scenario-Based Questions

Expect to face scenario-based questions that assess your problem-solving abilities and decision-making skills. Think about past challenges you've faced in clinical trials or medical affairs and how you navigated them. This will help illustrate your critical thinking and adaptability.

Clinical Development Medical Director - EMEA / UK
Dianthus Therapeutics, Inc.
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