At a Glance
- Tasks: Lead and oversee multiple clinical trials, ensuring medical accountability and safety.
- Company: Join a leading biopharmaceutical company dedicated to innovative cancer treatments.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Dynamic role with potential for international travel and collaboration with top experts.
- Why this job: Make a real difference in oncology by shaping clinical strategies and protocols.
- Qualifications: MD required with 5+ years of clinical trials experience and strong leadership skills.
The predicted salary is between 100000 - 150000 € per year.
The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, managing Phase 1 to Phase 3 studies with demonstrated decision making capabilities. The role has matrix management responsibilities across the internal and external network and provides medical and scientific expertise to cross‑functional BMS colleagues.
Responsibilities
- Medical Monitoring
- Team Leadership & Collaboration – Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT), partnering with Clinical Scientists to provide medical oversight on protocol development, including inclusion/exclusion criteria and safety considerations.
- Medical Monitoring & Safety – Lead medical and eligibility data reviews, assess safety‑related serious adverse events in partnership with Worldwide Patient Safety, and oversee site interactions and safety narratives.
- GCP & Compliance – Uphold all GCP obligations for clinical conduct, safety management guidelines, and maintain up‑to‑date required training.
- Clinical Development Expertise & Strategy
- Clinical Strategy & Protocol Design – Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols, focusing on drug/asset knowledge, disease area science, and regulatory targets.
- Medical Oversight & Accountability – Provide medical accountability across a group of studies, leading benefit/risk analyses within a matrix team environment alongside Clinical Scientists.
- Study Execution & Delivery – Partner with Clinical Scientists to support all aspects of study delivery, including site activation, enrollment, and adjudication of protocol violations and deviations.
- Stakeholder Engagement & Thought Leadership – Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design.
- Scientific Expertise & Education – Maintain deep, up‑to‑date knowledge of the disease area through conference attendance and literature review, staying informed on the competitive landscape and providing ongoing protocol‑specific medical education to study teams and investigators.
- Health Authority Interactions & Publications
- Health Authority & Advisory Engagement – Serve as the medical point of expertise in key Health Authority interactions and advisory board meetings.
- Regulatory Writing & Submissions – Author and draft clinical content for CSRs, regulatory reports, briefing books, and submission documents, including clinical narratives, in partnership with Clinical Scientists.
Qualifications and Experience
- MD required (or equivalent).
- Five or more years of industry experience and/or clinical trials experience.
- Ability to communicate information clearly and lead presentations in scientific and clinical settings.
- Subspecialty training in an applicable therapeutic area desired.
- Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation.
- Expertise in the drug development process and in executing an effective clinical plan and protocols.
- Strong leadership skills with proven ability to lead and work effectively in a team environment.
- Domestic and international travel may be required.
Director, Global Clinical Physician, Oncology in Uxbridge employer: Bristol Myers Squibb
Bristol Myers Squibb is an exceptional employer, offering a dynamic work environment that fosters collaboration and innovation in the field of oncology. With a strong commitment to employee growth, we provide extensive training opportunities and encourage participation in cutting-edge research, ensuring our team members are at the forefront of medical advancements. Located in a vibrant area, our culture prioritises inclusivity and support, making it an ideal place for professionals seeking meaningful and rewarding careers in clinical development.
StudySmarter Expert Advice🤫
We think this is how you could land Director, Global Clinical Physician, Oncology in Uxbridge
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to oncology. Building relationships can open doors that you didn’t even know existed.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, don’t hold back on sharing your knowledge. Discuss recent advancements in clinical trials or share insights from your experience. This shows you’re not just a candidate; you’re a thought leader!
✨Prepare for Interviews
Research the company and its recent projects thoroughly. Be ready to discuss how your background aligns with their goals, especially in clinical development and safety management. Confidence is key, so practice makes perfect!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at StudySmarter.
We think you need these skills to ace Director, Global Clinical Physician, Oncology in Uxbridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that align with the Director, Global Clinical Physician role. Highlight your medical oversight experience and any leadership roles you've held in clinical trials.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology and how your background makes you the perfect fit for this position. Don’t forget to mention your experience with GCP and compliance!
Showcase Your Teamwork Skills:Since this role involves collaboration with various teams, be sure to include examples of how you've successfully worked in a team environment. Highlight any cross-functional projects where you’ve made a significant impact.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at Bristol Myers Squibb
✨Know Your Clinical Trials Inside Out
Before the interview, dive deep into the specifics of clinical trials, especially in oncology. Familiarise yourself with Phase 1 to Phase 3 studies and be ready to discuss your experience managing these phases. This will show that you’re not just knowledgeable but also passionate about the field.
✨Showcase Your Leadership Skills
As a Director, you'll need to demonstrate strong leadership capabilities. Prepare examples of how you've successfully led teams in previous roles, particularly in a matrix management environment. Highlight your ability to collaborate with cross-functional teams and how you’ve contributed to study delivery.
✨Be Ready for Medical Oversight Questions
Expect questions around medical monitoring and safety management. Brush up on your knowledge of GCP obligations and safety-related serious adverse events. Be prepared to discuss how you’ve handled these aspects in past roles, as this will be crucial for the position.
✨Engage with Stakeholders
Think about how you’ve built relationships with principal investigators and key opinion leaders. Be ready to share specific examples of how you’ve engaged with stakeholders to inform clinical program design. This will demonstrate your ability to lead and influence in a clinical setting.
