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- Tasks: Negotiate complex contracts for global clinical trials and manage legal risks.
- Company: Leading healthcare organisation in London with a dynamic legal team.
- Benefits: Competitive salary, professional development, and a chance to work globally.
- Why this job: Join a global leader and make an impact in the healthcare sector.
- Qualifications: Dual-qualified in US and European law with experience in high-value contracts.
- Other info: Exciting opportunity for career growth in a fast-paced environment.
The predicted salary is between 43200 - 72000 £ per year.
A leading healthcare organization in London is seeking a Senior Legal Counsel who is dual-qualified in US and European law. In this role, you will negotiate complex contracts related to clinical trials and manage legal risks in a global environment.
Ideal candidates will have significant experience in negotiating high-value contracts and be well-versed in IP, data privacy, and competition laws. This is an excellent opportunity to join a global leader in a dynamic legal position.
Dual-Qualified Senior Legal Counsel – Global Clinical Trials employer: Graff Search
Contact Detail:
Graff Search Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Dual-Qualified Senior Legal Counsel – Global Clinical Trials
✨Tip Number 1
Network like a pro! Reach out to your connections in the legal field, especially those who have experience with clinical trials. They might know about opportunities that aren't advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your negotiation skills. Be ready to discuss specific examples of high-value contracts you've handled and how you navigated legal risks in a global context.
✨Tip Number 3
Showcase your dual-qualification! Make sure to highlight your expertise in both US and European law during conversations. This unique skill set is a big plus for roles involving international legal frameworks.
✨Tip Number 4
Don't forget to apply through our website! We make it easy for you to find and apply for roles that match your skills, so take advantage of it and get your application in!
We think you need these skills to ace Dual-Qualified Senior Legal Counsel – Global Clinical Trials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your dual-qualification in US and European law. We want to see your experience with negotiating high-value contracts, especially in the context of clinical trials.
Showcase Relevant Experience: When writing your cover letter, focus on your significant experience in IP, data privacy, and competition laws. We’re looking for candidates who can demonstrate their expertise in these areas.
Be Clear and Concise: In your application, clarity is key! Use straightforward language to explain your legal experience and how it relates to the role. We appreciate a well-structured application that gets straight to the point.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for this exciting opportunity.
How to prepare for a job interview at Graff Search
✨Know Your Legal Stuff
Make sure you brush up on both US and European law, especially around clinical trials. Be ready to discuss specific cases or examples where you've successfully navigated complex legal issues, particularly in IP, data privacy, and competition laws.
✨Showcase Your Negotiation Skills
Prepare to share detailed stories about high-value contracts you've negotiated. Highlight your strategies, the challenges you faced, and how you overcame them. This will demonstrate your capability to handle the complexities of the role.
✨Understand the Company’s Mission
Research the healthcare organisation thoroughly. Understand their values, recent developments, and how they approach global clinical trials. This knowledge will help you tailor your answers and show that you're genuinely interested in contributing to their mission.
✨Ask Insightful Questions
Prepare thoughtful questions that reflect your understanding of the role and the industry. Inquire about their approach to managing legal risks in clinical trials or how they stay compliant with evolving regulations. This shows your proactive mindset and engagement.
