Clinical Director

Clinical Director

Full-Time 80000 - 100000 ÂŁ / year (est.) No home office possible
SEC Life Sciences

At a Glance

  • Tasks: Lead innovative clinical development programmes for Alzheimer's disease and translate science into impactful strategies.
  • Company: Global biopharmaceutical organisation focused on neurodegenerative diseases.
  • Benefits: Hybrid work model, competitive contract terms, and opportunity to make a real difference.
  • Other info: Dynamic global environment with opportunities for professional growth and collaboration.
  • Why this job: Join a high-visibility role and contribute to transformative therapies for patients in need.
  • Qualifications: MD or MD/PhD with 5+ years in clinical research and Phase II-III experience.

The predicted salary is between 80000 - 100000 ÂŁ per year.

An innovative global biopharmaceutical organisation is seeking an experienced Medical Director - Neurodegenerative Diseases to support late-stage clinical development programmes in CNS, with a primary focus on Alzheimer's disease. This role offers the opportunity to contribute to pivotal Phase III programmes aimed at addressing significant unmet medical needs in neurodegeneration. You will play a central role in translating cutting‑edge science into high‑impact clinical strategies, helping to bring potentially transformative therapies to patients. This is a high‑visibility, cross‑functional leadership position within a global matrix environment.

Key Responsibilities

  • Support the design and execution of global clinical development strategies across all phases, with strong emphasis on Phase III programmes
  • Provide medical monitoring for ongoing interventional clinical trials
  • Contribute to protocol development, study design, and data interpretation
  • Partner closely with cross‑functional teams including Clinical Operations, Safety, Biostatistics, Regulatory Affairs, Clinical Pharmacology, Biomarkers, and Research
  • Support preparation for regulatory interactions and health authority engagements
  • Participate in advisory boards and engage with external investigators and key opinion leaders
  • Translate clinical data into strategic development decisions

Candidate Profile

Essential

  • MD or MD/PhD (medical degree required)
  • Minimum 5 years' experience in longitudinal clinical research, including hands‑on clinical trial experience (industry or academic setting)
  • Strong experience supporting or leading Phase II‑III development programmes, with particular focus on Phase III
  • Experience in medical monitoring of interventional studies
  • Proven ability to work effectively within global, cross‑functional matrix teams
  • Experience interfacing with regulatory authorities and external stakeholders
  • Excellent written and verbal scientific communication skills

Desirable

  • Direct experience in neurodegenerative diseases, particularly Alzheimer's disease
  • Experience designing late‑stage CNS development strategies
  • Prior experience within a global pharmaceutical or biotechnology organisation
  • Involvement in regulatory submissions
  • Peer‑reviewed publications in neurology or neurodegeneration

Who This Role Would Suit

  • Brings strong late‑stage CNS clinical development expertise
  • Is confident in medical monitoring and protocol design
  • Operates effectively in a complex, global matrix structure
  • Is comfortable engaging with regulators and external experts
  • Combines scientific rigour with strategic thinking

Work Arrangement & Contract Details

  • Contract position Outside IR35
  • Hybrid working: 2 days per week onsite in the Welwyn Garden City area

If you are passionate about advancing innovation in neurodegenerative disease and want to contribute to high‑impact late‑stage programmes, we encourage you to apply.

Clinical Director employer: SEC Life Sciences

As a leading global biopharmaceutical organisation, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in the field of neurodegenerative diseases. With a strong emphasis on professional growth, we offer extensive development opportunities and the chance to work alongside top experts in a hybrid environment, allowing for flexibility while contributing to groundbreaking clinical strategies aimed at transforming patient care. Join us in Welwyn Garden City, where your expertise will be valued and your contributions will directly influence the future of healthcare.
SEC Life Sciences

Contact Detail:

SEC Life Sciences Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Director

✨Tip Number 1

Network like a pro! Reach out to professionals in the neurodegenerative diseases field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Director role.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of Alzheimer's disease and recent advancements in clinical trials. We recommend having specific examples ready to showcase your experience in Phase II-III development programmes.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your passion for neurodegenerative diseases. We suggest using our website to find roles that truly excite you and match your expertise.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We believe showing genuine interest can set you apart from other candidates.

We think you need these skills to ace Clinical Director

Medical Monitoring
Clinical Trial Experience
Phase II-III Development Programmes
Protocol Development
Data Interpretation
Cross-Functional Team Collaboration
Regulatory Affairs Interaction
Scientific Communication Skills
Neurodegenerative Diseases Knowledge
CNS Development Strategies
Regulatory Submissions Experience
Peer-Reviewed Publications
Strategic Thinking
Adaptability in Global Matrix Structures

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of Clinical Director. Highlight your experience in neurodegenerative diseases and any relevant clinical trial work. We want to see how your background aligns with the key responsibilities outlined in the job description.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about advancing innovation in neurodegenerative diseases. We love seeing candidates who can connect their personal motivations with our mission at StudySmarter.

Showcase Your Communication Skills: Since excellent written communication is essential for this role, make sure your application is clear and concise. We appreciate well-structured documents that reflect your ability to convey complex scientific 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. Plus, it shows you’re proactive and engaged!

How to prepare for a job interview at SEC Life Sciences

✨Know Your Stuff

Make sure you brush up on the latest research and developments in neurodegenerative diseases, especially Alzheimer's. Being able to discuss recent studies or breakthroughs will show your passion and expertise in the field.

✨Showcase Your Experience

Prepare specific examples from your past roles that highlight your experience with Phase II-III development programmes. Be ready to discuss how you've contributed to clinical trials and any challenges you've overcome in medical monitoring.

✨Engage with Cross-Functional Teams

Since this role involves working closely with various teams, think of instances where you've successfully collaborated with different departments. Highlight your ability to communicate effectively and build relationships across a global matrix environment.

✨Prepare for Regulatory Discussions

Familiarise yourself with the regulatory landscape related to neurodegenerative diseases. Be prepared to discuss your experience interfacing with regulatory authorities and how you've navigated submissions or health authority engagements in the past.

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