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- Tasks: Lead clinical studies and provide expert advice on drug development in aesthetics.
- Company: Join a leading pharmaceutical company focused on innovative aesthetic solutions.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real impact in the aesthetic field and shape the future of drug development.
- Qualifications: 5+ years in clinical research with strong communication and collaboration skills.
- Other info: Dynamic work environment with opportunities to engage with senior management.
The predicted salary is between 72000 - 108000 £ per year.
Summary & Purpose of the Position
Main Responsibilities & Technical Competencies
- Leads and/or participates in marketing and clinical/medical advisory panels, steering committees and investigator meetings.
- Remains up to date with current information on pharmaceutical regulations, guidelines, and practices and therapeutic area knowledge and ensures consistent best practice across all activities.
- Provides expert scientific clinical development advice leadership to the project teams for the development of Phase I-IV clinical programs.
- Leads development of clinical studies and reviews clinical protocols, related documents, and clinical study reports for scientific and operational accuracy.
- Participates in drug safety surveillance for Development projects.
- Develop and demonstrate expertise in data review and interpretation to deliver meaningful efficacy and safety conclusions.
- Demonstrate the ability to interpret conclusions in context of product profiles and medical practice to create key messages, in collaboration with key stakeholders.
- Expertise in aesthetic drug development highly desired, but not required.
- Demonstrated in-depth understanding of drug development and pharmaceutical marketing within therapy area.
- Working knowledge of regulations relating to drug development and promotional activities.
- Demonstrated ability to communicate and plan effectively with other Ipsen departments and to respond to inquiries or complaints from customers.
- Demonstrated ability to effectively present information to senior management, employees at all levels of the organization, and external audiences.
- 5+ years experience of clinical research and organizational management within the pharmaceutical industry, a CRO, or similar organization.
- Demonstrated ability to collaborate in a matrixed environment.
- Experience in submissions of IND/CTX/NDA/MAA and interactions with Regulatory authorities, and/or experience in designing and conducting Phase I-III clinical trials; and/or significant late-stage development research.
Director, Clinical Science, Aesthetics in London employer: Ipsen Group
Contact Detail:
Ipsen Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Clinical Science, Aesthetics in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical science and aesthetics fields on LinkedIn. Join relevant groups and participate in discussions to get your name out there and show off your expertise.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of drug development regulations and practices. Be ready to discuss how your experience aligns with the role, especially in leading clinical studies and collaborating with cross-functional teams.
✨Tip Number 3
Don’t just wait for job openings to pop up! Keep an eye on our website and apply directly through it. This shows initiative and gives you a better chance of getting noticed by our recruiters.
✨Tip Number 4
Follow up after interviews with a thank-you email. Mention specific points from your conversation to remind them why you’re the perfect fit for the Director role. It’s a small gesture that can make a big impact!
We think you need these skills to ace Director, Clinical Science, Aesthetics in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Director, Clinical Science role. Highlight your expertise in clinical research and any relevant experience in aesthetic drug development to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this position and how your background makes you the perfect fit. Don’t forget to mention your understanding of drug development regulations and your ability to collaborate effectively.
Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just responsibilities. Use metrics where possible to demonstrate your impact in previous roles, especially in clinical trials or regulatory submissions.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at Ipsen Group
✨Know Your Stuff
Make sure you’re well-versed in the latest pharmaceutical regulations and guidelines. Brush up on your knowledge of clinical development, especially in aesthetics if you can. This will show that you’re not just interested in the role but also committed to staying updated in the field.
✨Showcase Your Experience
Prepare to discuss your past experiences in clinical research and organisational management. Be ready to share specific examples of how you've led clinical studies or collaborated in a matrixed environment. This will help demonstrate your capability to handle the responsibilities of the Director position.
✨Communicate Clearly
Practice articulating complex scientific concepts in a way that’s easy to understand. You’ll need to present information to senior management and external audiences, so being able to convey your ideas clearly is crucial. Consider doing mock interviews to refine your communication skills.
✨Engage with Key Stakeholders
Think about how you can effectively collaborate with various departments and stakeholders. Prepare examples of how you’ve successfully worked with others in the past, especially in drug safety surveillance or regulatory submissions. This will highlight your ability to build relationships and work as part of a team.
