Senior Clinical Development Medical Director - Renal in London

Senior Clinical Development Medical Director - Renal in London

London Full-Time 100000 - 130000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead renal clinical development programs from strategy to execution, ensuring rigorous decision-making.
  • Company: Join Novartis, a leader in innovative healthcare with a commitment to diversity and inclusion.
  • Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
  • Other info: Dynamic leadership role with opportunities for career advancement in a supportive environment.
  • Why this job: Make a real impact in renal drug development and collaborate with global experts.
  • Qualifications: MD or equivalent, 10+ years in clinical research, and expertise in renal disease.

The predicted salary is between 100000 - 130000 £ per year.

The Senior Clinical Development Medical Director (Sr CDMD) will lead the end-to-end strategy and execution of assigned renal clinical development program(s) across the full Research, Development and Commercial (RDC) continuum; from early development through pivotal/registrational phases. This is a key leadership role requiring hands-on experience in both early and late phase renal drug development. With the ability to translate emerging data into a clear clinical and regulatory path, drive delivery in a global matrix, and ensure rigorous benefit-risk decision making throughout the program lifecycle.

Major Accountabilities

  • Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program.
  • Leading development of clinical sections of trial and program level regulatory documents.
  • Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable.
  • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues.
  • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas.
  • As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards.
  • May work with BR (Biomedical Research/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed.

Minimum Requirements

  • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; clinical practice experience 4 years (including residency) and board certification or eligibility in disease area preferred.
  • Minimum of 10 years of experience in clinical research or drug development.
  • Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV is required.
  • Working knowledge of renal disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports.
  • Demonstrated ability to establish effective scientific partnerships with key stakeholders.
  • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes.
  • Previous global people management experience is preferred, though this may include management in a matrix environment.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Senior Clinical Development Medical Director - Renal in London employer: Novartis UK

At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior Clinical Development Medical Director in the renal field, you will have the opportunity to lead groundbreaking clinical programs while benefiting from our commitment to employee growth through continuous learning and development initiatives. Our global presence ensures that you will work alongside diverse teams, driving impactful change in patient care and making a meaningful difference in the communities we serve.

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Contact Details:

Novartis UK Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Clinical Development Medical Director - Renal in London

Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream role.

Tip Number 2

Prepare for interviews by researching the company and its culture. Understand their recent projects and challenges, especially in renal drug development. We want you to show them you’re not just another candidate, but someone who’s genuinely interested in their mission.

Tip Number 3

Practice your pitch! Be ready to explain how your experience aligns with the role of Senior Clinical Development Medical Director. We suggest rehearsing common interview questions and your responses so you can confidently showcase your expertise.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. Let’s get you one step closer to that leadership role!

We think you need these skills to ace Senior Clinical Development Medical Director - Renal in London

Clinical Leadership
Regulatory Document Development
Clinical Trial Execution
Safety Management
Clinical Development Planning
Stakeholder Engagement
Renal Disease Knowledge

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to highlight your experience in renal drug development and clinical research. We want to see how your background aligns with the key responsibilities of the Senior Clinical Development Medical Director role.

Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your leadership in clinical trials and how you've driven successful outcomes in previous projects.

Showcase Your Expertise:Don’t shy away from showcasing your knowledge in renal disease and clinical trial processes. We’re looking for someone who can interpret and present data effectively, so make sure to highlight relevant experiences.

Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensure it gets the attention it deserves!

How to prepare for a job interview at Novartis UK

Know Your Stuff

Make sure you brush up on your knowledge of renal disease and drug development. Be ready to discuss specific clinical trials you've worked on and how they relate to the role. This shows you're not just familiar with the theory but have practical experience too.

Showcase Your Leadership Skills

As a Senior Clinical Development Medical Director, you'll need to demonstrate your leadership abilities. Prepare examples of how you've led teams or projects in the past, especially in a global matrix environment. Highlight your ability to drive execution and make tough decisions.

Prepare for Regulatory Discussions

Since this role involves developing regulatory documents, be prepared to discuss your experience with these processes. Familiarise yourself with GCP and clinical trial design, and think about how you've contributed to safety reporting in previous roles.

Engage with Stakeholders

This position requires effective communication with various stakeholders. Think of examples where you've successfully built scientific partnerships or collaborated with cross-functional teams. Show that you can translate complex data into actionable insights for different audiences.