At a Glance
- Tasks: Lead oncology clinical development strategy and oversee global medical teams for emerging indications.
- Company: Dynamic pharmaceutical company focused on innovative oncology solutions.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Join a collaborative environment with a focus on innovation and excellence.
- Why this job: Shape the future of oncology and make a real impact in patient care.
- Qualifications: Extensive oncology experience, strategic thinking, and strong leadership skills.
The predicted salary is between 80000 - 100000 £ per year.
This hybrid, full-time position requires onsite presence at Bourne office in London, UK, 1 day per quarter. The role is offered on a hybrid basis. Reports to the Global Head Oncology Medical. The Head of Emerging Indications is a senior leader in Oncology Medical Development, accountable for shaping and executing clinical development strategy across emerging disease areas, with a strong focus on enabling enterprise growth through entry into new indications. This role provides leadership and oversight to multiple Global Medical Leads and drives delivery excellence across a portfolio of early- and late-stage programs. The leader helps define future portfolio direction through disease cluster strategy and active participation in business development activities. This is a permanent full-time position.
Responsibilities
- Portfolio Leadership and Emerging Indications Strategy
- Define and lead disease cluster strategies to enable entry into new and emerging oncology indications, aligned with enterprise priorities.
- Identify and shape opportunity spaces, integrating internal and external insights.
- Serve as a key thought partner in portfolio prioritization and long-term disease cluster strategy.
- Drive strategic decisions to ensure sustainable portfolio growth and differentiation.
- Clinical Development Leadership and Execution Excellence
- Provide oversight and direction to Global Medical Leads to ensure high-quality, timely execution of clinical programs.
- Guide design, review, and governance of clinical study protocols, ensuring scientific rigor, feasibility, and regulatory alignment.
- Ensure delivery of high-quality, credible data to support regulatory submissions, publications, and lifecycle strategies.
- Embed a culture of accountability, urgency, and excellence in execution across programs.
- Ensure optimal resource planning and deployment across the Emerging Indications portfolio.
- Cross-Functional, End-to-End Leadership and Integration
- Ensure integrated, end-to-end development strategies that align with regulatory and commercial objectives through seamless collaboration across Research, Early Development, Clinical Operations, Regulatory, Quantitative Sciences, Safety, Medical Affairs, and Commercial.
- Business Development and External Engagement
- Play a key leadership role in evaluation of in-licensing, out-licensing, and partnership opportunities.
- Provide Medical Development expertise in due diligence, asset valuation, and integration planning.
- Contribute to strategy development for multi-track business development initiatives within Oncology.
- Governance, Compliance, and Operational Excellence
- Participate/Lead governance forums, providing a strong Medical Development perspective.
- Ensure adherence to ICH, GCP, and company policies across all development activities.
- Contribute to the establishment and continuous improvement of processes and SOPs.
Qualifications
- Extensive experience working within the pharmaceutical/biotechnology industry, including significant oncology clinical development experience across phases.
- Strategic thinker with the ability to translate vision into actionable plans with accountability and urgency, integrating diverse perspectives.
- Demonstrated experience leading global development teams and complex programs.
- Proven ability to develop and execute clinical development strategies and regulatory submissions.
- Strong cross-functional expertise spanning clinical, regulatory, safety, and commercial considerations.
- Experience contributing to or leading business development assessments and due diligence.
- Established track record in people leadership, talent development, and change management.
- Exceptional communication skills with the ability to convey complex concepts clearly to diverse stakeholders with cultural awareness.
- Advanced degree in life sciences, medicine, or related field; MD degree with board certification and clinical oncology practice experience.
- Experience in thoracic oncology.
- Exposure to related and complimentary functional areas (medical affairs, safety science, etc.).
- Experience managing multi-year budgets and resource allocation across complex portfolios.
Medical Development Head of Emerging Indications, Executive Director in City of Westminster employer: Astellas Pharma
As a leading player in the oncology sector, our company offers an exceptional work environment that fosters innovation and collaboration. With a strong commitment to employee growth, we provide ample opportunities for professional development and leadership within a supportive culture that values accountability and excellence. Located in the vibrant city of London, our hybrid working model allows for flexibility while ensuring that our team remains engaged and connected, making it an ideal place for those seeking meaningful and rewarding careers in medical development.
StudySmarter Expert Advice🤫
We think this is how you could land Medical Development Head of Emerging Indications, Executive Director in City of Westminster
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We think you need these skills to ace Medical Development Head of Emerging Indications, Executive Director in City of Westminster
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 Astellas Pharma!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Astellas Pharma that you're not just a fit for the job but also a safety-conscious candidate!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Astellas Pharma, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Astellas Pharma
✨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 Astellas Pharma 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.
✨Know Their Products
Take some time to familiarise yourself with Astellas Pharma’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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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.
