At a Glance
- Tasks: Lead clinical development strategies in oncology and immune-oncology, collaborating globally.
- Company: Join GE HealthCare, a leader in medical technology and digital solutions.
- Benefits: Enjoy flexible work options, competitive salary, and a supportive culture.
- Why this job: Make a real impact on patient care while working with innovative products.
- Qualifications: Medical degree and experience in oncology required; GCP knowledge is essential.
- Other info: Remote work available; travel may be necessary.
The predicted salary is between 72000 - 108000 £ per year.
Job Location: Great Britain, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: Director
Job Description Summary
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Roles and Responsibilities
- To provide clinical leadership in cross-functional projects and product/project teams
- To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
- To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
- To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
- To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
- To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
- To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
- To collaborate with multiple functions for identifying and selecting innovative products for development
- To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
Required Qualifications
- Medical Degree
- Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
- A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
- Proven experience in Good Clinical Practice (GCP) Clinical trials
- Must be willing to travel as required.
- Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
Desired Characteristics
- Excellent interpersonal, organization, communication, influencing skills.
- Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
- Experience in scientific publications/communication
- Experience managing complex projects and/or across global regions desirable.
- Good team player with global mindset
- Ability to work independently and with rigor
- Good process knowledge, experience, and skills
- Customer savvy.
Inclusion and Diversity
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
Total Rewards
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
About Us
GE HealthCare is one of the global leaders in medical technology and digital solutions. It enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services. With over 100 years of experience in healthcare and approximately 47,000 employees worldwide, the company is at the centre of an ecosystem that is working towards precision medicine.
Medical Director- Oncology / Directeur Médical en Oncologie (Basé à London) employer: Golden Bees
Contact Detail:
Golden Bees Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Director- Oncology / Directeur Médical en Oncologie (Basé à London)
✨Tip Number 1
Network with professionals in the oncology and pharmaceutical sectors. Attend industry conferences, webinars, and local meetups to connect with key opinion leaders (KOLs) and other experts who can provide insights and potentially refer you to opportunities at StudySmarter.
✨Tip Number 2
Familiarise yourself with the latest advancements in molecular imaging and oncology. Being well-versed in current trends and technologies will not only enhance your discussions but also demonstrate your commitment and expertise during interviews.
✨Tip Number 3
Prepare to discuss your experience with cross-functional teams. Highlight specific projects where you collaborated with regulatory, clinical, and commercial functions, as this role requires extensive interaction across various departments.
✨Tip Number 4
Showcase your leadership skills by providing examples of how you've successfully managed complex projects or teams in the past. This will be crucial in demonstrating your capability to lead clinical development strategies effectively.
We think you need these skills to ace Medical Director- Oncology / Directeur Médical en Oncologie (Basé à London)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in oncology and clinical development. Emphasise any leadership roles you've held and specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: In your cover letter, express your passion for oncology and molecular imaging. Discuss how your background and skills make you a perfect fit for leading clinical development strategies, and mention any relevant achievements or experiences.
Highlight Key Qualifications: Clearly outline your medical degree and substantial experience in the pharmaceutical or biotech industry. Mention your familiarity with Good Clinical Practice (GCP) and any specific experience with imaging diagnostics to strengthen your application.
Showcase Interpersonal Skills: Since the role requires excellent communication and influencing skills, provide examples of how you've successfully managed cross-functional teams or collaborated with key opinion leaders (KOLs) in your previous roles.
How to prepare for a job interview at Golden Bees
✨Showcase Your Clinical Expertise
As a Medical Director in Oncology, it's crucial to demonstrate your extensive knowledge and experience in clinical development. Be prepared to discuss specific projects you've led, particularly in oncology and immune-oncology, and how they relate to the role.
✨Highlight Cross-Functional Collaboration
This position requires significant interaction across various functions. Share examples of how you've successfully collaborated with teams such as regulatory affairs, compliance, and pharmacovigilance to achieve project goals.
✨Prepare for Technical Questions
Expect to face technical questions related to Good Clinical Practice (GCP) and clinical trial management. Brush up on your knowledge of these areas and be ready to explain how you've applied them in your previous roles.
✨Demonstrate Leadership Skills
As a director, showcasing your leadership abilities is essential. Prepare to discuss your experience in managing complex projects and leading teams, as well as how you influence and communicate with key opinion leaders (KOLs) and external experts.