At a Glance
- Tasks: Lead medical strategy and execution for innovative clinical development programmes.
- Company: Join UCB, a global biopharmaceutical company focused on neurology and immunology.
- Benefits: Enjoy a supportive culture, hybrid work, and opportunities for personal growth.
- Other info: Collaborate with diverse teams and engage with global stakeholders.
- Why this job: Make a real impact on patients' lives through strategic leadership in clinical development.
- Qualifications: Medical Degree and experience in clinical development or medical affairs required.
The predicted salary is between 80000 - 100000 £ per year.
Make your mark for patients. We are looking for a strategic, collaborative, and science-driven Clinical Development Physician (Director) to join our Global Clinical Development team in Slough, UK.
About the role: As a Clinical Development Physician, you will be accountable for the medical integrity and strategic direction of clinical development programs. Acting as the medical expert for assigned assets, you will ensure the program reflects current scientific knowledge, clinical best practices, and evolving healthcare landscapes. You will play a critical leadership role in shaping development strategies, driving execution, and delivering high-quality clinical outcomes that support global patient access.
Who you’ll work with: You will collaborate with cross-functional global teams, including clinical development, medical affairs, regulatory, and biometrics, as well as engage with external stakeholders such as investigators, regulatory authorities, and key opinion leaders. You may also lead clinical development teams or programs, contributing to both strategic leadership and operational execution.
What you’ll do:
- Lead medical strategy and execution for clinical development programs
- Ensure scientific integrity across protocols, reports, and development plans
- Provide medical oversight, monitoring, and benefit-risk assessment
- Contribute to regulatory submissions and global health authority interactions
- Build and maintain relationships with investigators and external stakeholders
- Represent the organization at scientific forums and conferences
Interested? For this role we’re looking for the following education, experience and skills:
Minimum Qualifications:
- Medical Degree (M.D.) with active licensure or equivalent
- Minimum 5 years’ experience in a clinical or academic setting (e.g., academic physician or investigator involved in clinical trials) or in medical affairs within the biopharmaceutical industry OR Minimum of 3 years’ experience in clinical development in the biopharmaceutical industry.
Preferred Qualifications:
- Advanced certification in pharmaceutical medicine
- Experience with regulators and health authorities
- Leadership in clinical development programs
- Strong knowledge of global clinical and regulatory requirements
- Ability to lead cross-functional, matrixed teams
- Excellent communication, presentation, and stakeholder management skills
- Experience collaborating with global and diverse teams
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us: UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us? At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Clinical Development Physician (UK) in Slough employer: UCB
UCB is an exceptional employer, offering a dynamic and inclusive work culture that prioritises collaboration and innovation in the biopharmaceutical sector. Located in Slough, UK, employees benefit from a hybrid-first approach, allowing for flexibility while fostering teamwork in local hubs. With a strong focus on personal growth and career development, UCB empowers its staff to make meaningful contributions towards improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Development Physician (UK) in Slough
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We think you need these skills to ace Clinical Development Physician (UK) in Slough
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 UCB!
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 UCB that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at UCB!
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 UCB, 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 UCB
✨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 UCB that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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 UCB’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.
✨Be Ready for Regulatory Scenarios
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.
