Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical strategy and ensure high-quality data interpretation in Neurology and Immunology trials.
- Company: Global organisation with a focus on innovative clinical development.
- Benefits: Competitive daily rate, remote work, and opportunity to shape clinical strategies.
- Why this job: Make a real impact in clinical research while working with top professionals in the field.
- Qualifications: Strong clinical data review experience and proven background in clinical development.
- Other info: Collaborative environment with opportunities for professional growth and networking.
CPL Life Sciences is supporting a global organisation in the search for an experienced Clinical Development Director to provide clinical, scientific, and strategic guidance across their major Neurology and Immunology development programme. This role plays a central part in shaping clinical strategy, ensuring high-quality data interpretation, and driving delivery across early- and mid-stage clinical trials.
The CDD will contribute to the development and refinement of clinical plans, lead or support the creation of protocol documents, and prepare clinical content for regulatory submissions. A core component of the position involves real-time review of clinical data in close collaboration with medical monitors, data management, and statistical functions to ensure robust data quality and clear clinical insight throughout the life of the study.
Key experience required:
- Strong clinical data review experience, working with medical monitors, data management, and statistics
- Proven background in clinical development, including protocol design and authorship
- Experience across early and late phases of clinical development
- Familiarity with regulatory document preparation and submission processes
- Ability to interpret, analyse, and communicate complex clinical and scientific data
- Experience supporting inspection readiness and QA interactions
- Strong understanding of safety monitoring, signal evaluation, and related documentation
- Demonstrated ability to work cross-functionally with internal and external stakeholders
- Established relationships with KOLs, particularly in Neurology (desirable)
- Experience overseeing outsourced studies and collaborating with CROs
Clinical Scientific Development Director in London employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Scientific Development Director in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those in neurology or immunology. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your clinical data review skills. Be ready to discuss your experience with protocol design and regulatory submissions. We want you to shine when it comes to showcasing your expertise!
✨Tip Number 3
Don’t forget to tailor your approach! When applying through our website, highlight your specific experiences in early and late-phase clinical development. Make it clear how your background aligns with the role of Clinical Scientific Development Director.
✨Tip Number 4
Stay proactive! Follow up after interviews to express your continued interest. A simple thank-you email can keep you top of mind and show that you're genuinely excited about the opportunity.
We think you need these skills to ace Clinical Scientific Development Director in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in clinical development, especially in Neurology or Immunology. We want to see how your background aligns with the key responsibilities mentioned in the job description.
Craft a Compelling Cover Message: Use the cover message to showcase your passion for the role and the unique skills you bring to the table. We love seeing candidates who can communicate their enthusiasm and fit for the position!
Highlight Relevant Experience: When detailing your experience, focus on your work with clinical data review, protocol design, and regulatory submissions. We’re looking for specific examples that demonstrate your expertise and ability to drive clinical strategy.
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 hear from you!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Clinical Data Inside Out
Make sure you brush up on your clinical data review experience. Be prepared to discuss specific examples where you've worked with medical monitors and data management teams. This will show that you can interpret and analyse complex data effectively.
✨Familiarise Yourself with Protocol Design
Since protocol design and authorship are key parts of the role, take some time to review your past experiences in this area. Be ready to share insights on how you've contributed to clinical plans and any challenges you've faced during protocol creation.
✨Understand Regulatory Processes
Get a good grasp of the regulatory document preparation and submission processes. You might be asked about your experience with these, so having a few examples ready will demonstrate your familiarity and readiness for the role.
✨Showcase Your Cross-Functional Collaboration Skills
This position requires working closely with various stakeholders. Think of instances where you've successfully collaborated with internal teams or external partners, especially in overseeing outsourced studies. Highlighting these experiences will show your ability to work effectively across functions.
