At a Glance
- Tasks: Lead clinical development in Neuroscience and oversee cross-functional teams.
- Company: Join Novartis, a global leader in innovative healthcare solutions.
- Benefits: Enjoy competitive rewards, professional growth opportunities, and a supportive work culture.
- Why this job: Make a real impact on patients' lives while collaborating with passionate experts.
- Qualifications: MD or PhD with 10+ years in clinical research; expertise in Neuroscience required.
- Other info: Remote work options available; join a community dedicated to breakthroughs in healthcare.
The predicted salary is between 72000 - 108000 £ per year.
Summary
As Global Program Clinical Head (GPCH), you are the clinical lead for Neuroscience, leading clinical development and contributing to overall strategy in collaboration with other functions, to ensure the development and implementation of the Clinical Development plan. You will lead a cross-functional team of specialists and align early development plans with the overall strategy, oversee licensing evaluations, and develop and execute the disease area strategy.
About the Role
Your Key Responsibilities:
- Responsible for clinical input to support Business Development & Licensing (BD&L) activities.
- The GPCH works to ensure early development plans and proof of concept studies are aligned with Development strategy.
- Serve as the Clinical Development Representative to drive transition of pre-PoC (Proof of Concept) projects to Development Decision Point (DDP)
- Contribute to Integrated Development Plan (IDP) in line with the Target Product Profile (TPP) which is designed for successful global regulatory approval/market access for one or more treatment indications and/or multiple programs.
- Drive creation and implementation of Clinical Development to support decision analysis and optimal resource allocation in program(s).
- Lead a cross functional team through the creation of clinical components of key documents (e.g., Clinical Trial Protocols, Investigator’s Brochures, Clinical Study Reports, regulatory documents including maintenance of product licenses, registration dossiers, value dossiers, pharmacoeconomic dossiers) with high quality and consistency.
- As the medical expert, lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards, patient advocacy groups), internal stakeholders (e.g., Research, Translational Medicine, Global Medical Affairs, Marketing, Health Economics & Outcomes Research), and internal decision boards
- Together with Patient Safety, ensure continuous evaluation of drug safety profile, including safety monitoring of clinical studies and signal detection from post-marketing surveillance.
- Support registration, market access, commercialization, and maintenance of product licenses (e.g., Core Data Sheet, Periodic Safety Update Report, clinical benefit-risk assessment for license renewals) for the compound(s)
- Plan and implement publication and clinical communication strategy in coordination with Global Medical Affairs and Medical Writing, and provide input into key external presentations
Role Requirements:
Essential Requirements:
- MD, or PH. D degree with 10+ years’ experience in clinical research or drug development in an industry environment spanning clinical activities in Phases I-III/IV, including submission dossiers.
- A passion for Neuroscience
- Advanced expertise in Neuroscience with ability to innovate in clinical development study designs, provide relevant evidence to decision-makers and to interpret, discuss and present clinical trial or section program level data
- Detailed knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory/clinical development process
- Demonstrated ability to establish strong scientific partnership with key stakeholders
- Demonstrated leadership and management skills with a documented track record of delivering high quality projects/submissions/trials in a global/matrix environment (including remote) in pharmaceutical or biotech industry
Desired Requirements:
- MD or equivalent, MD or MD/PhD in Neurology, Experience in Cell & Gene, Rare or Neuromuscular, Neurodegenerative diseases, Neuroinflammation of interest
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture(link is external)
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards(link is external)
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Global Program Clinical Head (Early GPCH NS) employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Program Clinical Head (Early GPCH NS)
✨Tip Number 1
Network with professionals in the Neuroscience field. Attend relevant conferences and seminars to meet key opinion leaders and potential colleagues. Building these connections can provide insights into the role and may even lead to referrals.
✨Tip Number 2
Stay updated on the latest trends and advancements in Neuroscience and clinical development. This knowledge will not only help you during interviews but also demonstrate your passion and commitment to the field.
✨Tip Number 3
Prepare to discuss your leadership experiences in detail. Be ready to share specific examples of how you've successfully led cross-functional teams and managed complex projects, as this is crucial for the Global Program Clinical Head role.
✨Tip Number 4
Familiarise yourself with Novartis' mission and values. Understanding their approach to patient care and innovation will help you align your responses during interviews and show that you're a good cultural fit for the company.
We think you need these skills to ace Global Program Clinical Head (Early GPCH NS)
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and requirements of the Global Program Clinical Head position. Tailor your application to highlight relevant experiences in clinical research and drug development, particularly in Neuroscience.
Highlight Relevant Experience: In your CV and cover letter, emphasise your 10+ years of experience in clinical research or drug development. Include specific examples of your leadership in cross-functional teams and any successful projects you've managed that align with the job description.
Showcase Your Passion for Neuroscience: Demonstrate your passion for Neuroscience in your application. Discuss any innovative study designs you have contributed to or how you've engaged with key stakeholders in this field. This will help convey your commitment to the role.
Proofread and Format: Ensure your application is free from errors and well-formatted. Use clear headings and bullet points to make it easy for the hiring team to read. A polished application reflects your attention to detail, which is crucial for this role.
How to prepare for a job interview at Novartis
✨Showcase Your Clinical Expertise
As a candidate for the Global Program Clinical Head, it's crucial to demonstrate your advanced knowledge in Neuroscience. Be prepared to discuss your experience in clinical research and drug development, particularly in Phases I-III/IV, and how it aligns with the company's goals.
✨Highlight Leadership Skills
This role requires strong leadership and management abilities. Share specific examples of how you've successfully led cross-functional teams in the past, focusing on your ability to deliver high-quality projects in a global or matrix environment.
✨Prepare for Stakeholder Engagement
You'll need to interact with various stakeholders, including regulatory authorities and key opinion leaders. Prepare to discuss your experience in building scientific partnerships and how you effectively communicate complex clinical data to different audiences.
✨Understand Regulatory Processes
A solid understanding of Good Clinical Practice and the regulatory landscape is essential. Brush up on your knowledge of clinical trial design and submission dossiers, and be ready to explain how you've navigated these processes in your previous roles.