Development Physician (Medical Director), Oncology
About Astellas
Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com.
Are you driven to make a real difference in the lives of patients?
We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.
Location and Working Environment
This is a permanent full-time position. This position is hybrid and will require you to be on-site 1 day per quarter at Bourne office in London, UK. The role is offered on a hybrid basis.
At Astellas we recognise that our employees enjoy having balance between their professional and home lives. We are proud of our hybrid approach which empowers you to have flexibility on whether to work from home or in the office.
This role reports to the Global Medical Portfolio Lead for Late Oncology.
Purpose & Scope
- As the Development Physician (Medical Director) you will be a core member of the clinical team, responsible for the design and execution of clinical trials, whilst serving as a Medical Monitor with oversight of safety monitoring and documentation.
- This role supports efficient trial execution and high-quality data collection to guide strategic decisions, contributing to clinical development initiatives, and providing scientific and medical training to internal and external stakeholders.
- At Astellas we recognise the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimise the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines.
Role and Responsibilities
- Serving as a Medical Monitor with responsibility for safety monitoring on clinical studies. Generating safety related documents, such as medical monitoring reports. Collaborating closely with the safety officer in writing and/or reviewing safety narratives, investigator letters, and other safety documentation for site-reported safety events.
- Partnering with Development Scientists responsible for the medical aspects of all study-related documents, including for example the clinical study protocol, informed consent forms, clinical database, safety committee charters and clinical study reports.
- Working with Development Scientists and Clinical Operation Leads to ensure efficient and streamlined execution of clinical trials and acquisition and interpretation of high-quality clinical data to inform program-level decision making and overall development strategies.
- Supporting functional level clinical development related initiatives as needed. Leading and/or participating in scientific and medical training to other team members and external clients, investigators, and other site staff as it pertains to assigned studies.
Required Qualifications
- MD or MD/PhD, or equivalent.
- Experience working within the pharmaceutical industry specifically in clinical trial design and execution in a bio-pharmaceutical development organisation or a balance of experience at an academic institution and a pharmaceutical company.
- Excellent verbal and written communication skills in English.
- Experience working in global teams and a global matrixed, remote working environment.
- Aware of cultural diversity and how to influence and manage in a multi-cultural organisation.
- Highest level of scientific integrity and impeccable work ethics.
Preferred Qualifications
- Board certified in Oncology or Oncology-related specialty
- Experience in solid tumours, preferably Gastro-Intestinal, Thoracic or Genito-Urinary
- Experience in late development oncology (Ph3)
- Direct experience leading global regulatory marketing authorisation submissions and defense of those submissions
What awaits you at Astellas?
- Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide.
- Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.
- Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.
- A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.
Our Organizational Values and Behaviours
- Impact
- Innovation
- Integrity
- One Astellas
- Accountability
- Courage
- Sense of Urgency
- Outcome Focus
Benefits
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help.
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