At a Glance
- Tasks: Lead global medical strategies for GI cancers and collaborate with cross-functional teams.
- Company: Join Jazz Pharmaceuticals, a biopharma innovator transforming patient lives.
- Benefits: Competitive salary, bonuses, flexible vacation, and comprehensive health benefits.
- Other info: Remote work opportunity with excellent career growth potential.
- Why this job: Make a real impact in oncology while working with a passionate team.
- Qualifications: 10+ years in Medical Affairs or Clinical Development, preferably in oncology.
The predicted salary is between 63000 - 77000 £ per year.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide.
The Senior Global Medical Director, Gastrointestinal Cancers is a key member of the Global Commercialization Organization Medical Affairs (GCOMA) Oncology team and reports to the VP, GCO Medical Affairs, Oncology. This is a strategic role with execution responsibilities, accountable for ensuring the needs and priorities of the US (as lead region) and EUR/INT regions are represented and addressed through engagement with key partners across Jazz. Working closely with regional Medical Affairs colleagues, the Senior Global Medical Director ensures a deep understanding of customer, patient, and healthcare system needs are represented consistently across global cross-functional discussions and decision-making forums.
Essential Functions/Responsibilities:
- Lead the GI Cancer Global Medical functional matrix team
- Partner closely with US and EUR/INT Medical Affairs teams to understand regional customer, patient, healthcare provider, and healthcare system needs and priorities
- Represent and advocate for medical perspectives within global cross-functional teams and governance forums, including CDT, LDT, PGC, and DPRC
- Contribute Medical Affairs expertise to inform early development activities, including Target Product Profile (TPP) development, clinical trial design and lifecycle planning based on regional insights and aligned future therapeutic landscape scenarios
- Ensure regional needs and insights are appropriately considered in clinical development discussions, evidence-generation activities, and lifecycle planning
- Maintain and apply a deep understanding of the competitive landscape to inform evidence generation strategy and internal development decisions
- Lead the development, maintenance, and execution of the Integrated Evidence Generation Plan (IEGP) for Solid Tumor Oncology Product, in BTC and Gastroesophageal Cancer and other GI malignancies as assigned
- Partner effectively across Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, HEOR, RWE, Commercial, and other cross-functional teams to support evidence generation and scientific exchange
- Lead and support evidence-generation activities, including investigator-sponsored studies, real-world evidence initiatives, health outcomes research, and Phase IV interventional studies, where appropriate
- Lead the development of the breast cancer medical narrative by identifying and advancing key analytic needs and informing the interpretation of pivotal trial data
- Provide Medical Affairs leadership and input into the Payor Value and Evidence Plan (GVEP)
- Lead development and execution of publication strategy and evidence dissemination plan in alignment with regional evidence needs and scientific priorities
- Support scientific communications, congress planning, advisory boards, and external engagement activities as required
- Act as a subject matter expert for internal cross-functional stakeholders
Required Knowledge, Skills, and Abilities:
- A minimum of 10 years of Medical Affairs, Clinical Development, or related pharmaceutical or biotechnology industry experience is required, preferably in oncology
- Experience in GI cancers and/or HER2-targeted therapies are strongly preferred
- Demonstrated experience developing and executing evidence-generation strategies, publication plans, and external scientific engagement activities
- Strong understanding of clinical research, evidence generation, and oncology drug development
- Proven ability to influence without authority and operate effectively within complex matrix organizations
- Strong strategic thinking coupled with excellent operational execution skills
- Excellent written, verbal, presentation, and stakeholder management skills
- Ability to build productive partnerships across regions and functions and effectively represent diverse stakeholder perspectives
- Demonstrated ability to manage multiple priorities and deliver high-quality outcomes in a fast-paced environment
- Experience in the lifecycle management of oncology indications strongly desired
- Evidence of success in matrix organizations and track record of high performing behaviors, including independent critical thinking, initiative, and execution under time pressure with competing priorities
- Self-awareness and emotional intelligence as demonstrated by prior experience navigating complex matrix environments successfully
Required/Preferred Education and Licenses:
- Advanced scientific or healthcare degree required (PharmD, PhD, MD, MBBS, Nurse Practitioner, PA, or equivalent)
- Experience in the delivery of oncology care preferred
Senior Director, Global Medical Director, GI Tumors in London employer: Jazz Pharmaceuticals
Jazz Pharmaceuticals is an exceptional employer, offering a dynamic work culture that prioritises innovation and collaboration in the biopharma industry. With a strong commitment to employee growth, we provide numerous opportunities for professional development and a competitive benefits package, including flexible paid vacation and comprehensive health insurance. Located in vibrant cities like London and Cambridge, our employees enjoy a stimulating environment that fosters creativity and teamwork while making a meaningful impact on patients' lives worldwide.
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We think this is how you could land Senior Director, Global Medical Director, GI Tumors in London
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We think you need these skills to ace Senior Director, Global Medical Director, GI Tumors in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Jazz Pharmaceuticals!
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How to prepare for a job interview at Jazz Pharmaceuticals
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Jazz Pharmaceuticals that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
