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- Tasks: Lead clinical trials and develop strategies for innovative rheumatology treatments.
- Company: Join Novartis, a global leader in healthcare dedicated to improving patient outcomes.
- Benefits: Enjoy flexible location options and a commitment to diversity and inclusion.
- Why this job: Make a real impact in healthcare while collaborating with top professionals in the field.
- Qualifications: MD or equivalent, with 4+ years of clinical practice and 5+ years in research.
- Other info: Opportunities for career development and participation in global initiatives.
The predicted salary is between 72000 - 108000 £ per year.
Join us to apply for the Clinical Development Medical Director - Rheumatology role at Novartis.
Job Summary
As our Clinical Development Medical Director in the Immunology Development Unit, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data.
About The Role
The Clinical Development Medical Director (CDMD) for Rheumatology is the clinical leader for program-level activities, such as submission activities and briefing books, or for large, complex trials under the leadership of the (Senior) GPCH. You may lead a section of a clinical program, such as an indication, a new formulation, or a specific development phase.
Your Responsibilities
- Provide clinical leadership and strategic medical input for project deliverables, including protocol sections, data review, regulatory documents, and publications.
- Drive execution of program sections in partnership with global functions, Trial Directors, and regional medical teams.
- Oversee scientific review of trial data; serve as study medical monitor if needed.
- Support safety monitoring and reporting, contributing to safety documents and collaboration with Patient Safety.
- Contribute to development standards and provide medical input for reviews and external interactions.
- Support transition of pre-PoC projects and collaborate with BD&L for target identification and due diligences.
- Ensure career development of team members through performance management, onboarding, training, and mentoring.
- Contribute to medical training and serve as a speaker for the franchise.
- Lead or participate in global initiatives for process improvement, training, and SOP development.
Minimum Requirements
- MD or equivalent medical degree; Board certification preferred.
- 4+ years of clinical practice experience; 5+ years in clinical research or drug development.
- Experience in all phases of clinical trials and advanced knowledge of the therapeutic area.
- Strong scientific partnership skills, GCP knowledge, and regulatory understanding.
- People management experience, preferably in a global matrix environment.
- Excellent communication, interpersonal, negotiation, and conflict resolution skills.
Location options include Basel, London, Barcelona, Madrid, or Dublin. Novartis is committed to diversity and inclusion, offering accommodations for applicants with disabilities.
Clinical Development Medical Director - Rheumatology employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Development Medical Director - Rheumatology
✨Tip Number 1
Network with professionals in the rheumatology field. Attend relevant conferences or webinars where you can meet people who work at Novartis or in similar roles. Building these connections can provide insights into the company culture and potentially lead to referrals.
✨Tip Number 2
Stay updated on the latest advancements in rheumatology and clinical development. Follow industry news, read recent publications, and engage in discussions on platforms like LinkedIn. This knowledge will not only help you during interviews but also demonstrate your passion for the field.
✨Tip Number 3
Prepare to discuss your leadership experience in clinical settings. Think of specific examples where you've successfully managed teams or projects, especially in a global context. Highlighting your ability to lead and mentor others will be crucial for this role.
✨Tip Number 4
Familiarise yourself with Novartis' values and mission. Understanding their commitment to diversity and inclusion, as well as their approach to patient safety, will allow you to align your responses during interviews and show that you're a good fit for their team.
We think you need these skills to ace Clinical Development Medical Director - Rheumatology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research and drug development, particularly in rheumatology. Emphasise your leadership roles and any specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that clearly articulates your passion for rheumatology and your vision for the role. Mention specific experiences that demonstrate your ability to lead clinical trials and collaborate with global teams.
Highlight Relevant Skills: In your application, focus on key skills such as scientific partnership, GCP knowledge, and people management. Provide examples of how you've successfully used these skills in previous roles.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents for any errors or inconsistencies. A polished application reflects your attention to detail and professionalism, which are crucial for this role.
How to prepare for a job interview at Novartis
✨Showcase Your Clinical Expertise
As a Clinical Development Medical Director, it's crucial to demonstrate your deep understanding of clinical trials and rheumatology. Be prepared to discuss your previous experiences in clinical research, highlighting specific projects where you provided strategic medical input.
✨Emphasise Leadership Skills
This role requires strong leadership capabilities. Share examples of how you've successfully managed teams or led projects in a global matrix environment. Discuss your approach to mentoring and developing team members, as this will be key to your success in the position.
✨Prepare for Regulatory Discussions
Given the importance of regulatory documents and compliance in this role, brush up on your knowledge of GCP and relevant regulations. Be ready to discuss how you've navigated regulatory challenges in past projects and your strategies for ensuring compliance.
✨Demonstrate Communication Skills
Excellent communication is vital for this position. Prepare to showcase your interpersonal skills by discussing how you've effectively communicated complex scientific information to diverse audiences, including stakeholders and regulatory bodies.
