At a Glance
- Tasks: Lead clinical contract compliance and support innovative research in a patient-focused environment.
- Company: Ipsen Pharma, a global biopharmaceutical leader dedicated to transformative medicines.
- Benefits: Empowering workplace culture, growth opportunities, and commitment to employee well-being.
- Other info: Join a diverse team that values inclusion and supports your unique journey.
- Why this job: Make a real impact on patients' lives while advancing your career in a dynamic field.
- Qualifications: Master's in Law and experience in clinical contracts or data privacy compliance required.
The predicted salary is between 63000 - 77000 £ per year.
About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavour every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success.
Job Description: Are you ready to lead and innovate in a dynamic, patient-focused biopharmaceutical company? Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life, providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.
Why Ipsen?
- Patient-Focused: The patient is at the heart of everything we do, and improving their outcomes is the deliverable of every strategy.
- Employee Care: We care for our employees, who are the ambassadors making a real difference.
- Bold Leadership: We attract and develop bold, agile, entrepreneurial individuals who take full ownership of their decisions.
- Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving, game-changing organization.
About the Role: The Clinical Contract Manager ensures that clinical research activities are conducted in full compliance with applicable legal, regulatory, contractual, and data privacy requirements, and oversees the Clinical Contract Associate (CCA) team activities. Positioned within Global Medical Clinical Operations / Clinical Excellence, you provide expert support and oversight on contracts managed by the department (clinical studies, managed access programs, contractors) and data protection matters, enabling compliant and efficient study execution while safeguarding patient data and Ipsen’s legal obligations.
Main Responsibilities:
- Clinical Contracts Compliance: Provide expert oversight and guidance on agreements, ensuring contractual content is fully compliant with applicable legal, regulatory, and data protection requirements.
- Data Privacy & GDPR Compliance: Act as the clinical data privacy champion for Global Medical Clinical Operations. Ensure compliance with GDPR and/or any applicable data protection laws for clinical studies, registries and Managed Access Programs. Review and support privacy-related documentation.
- Advisory, Training & Operational Support: Act as a trusted advisor to Clinical Operations teams on clinical contracts and data privacy topics. Provide pragmatic, solution-oriented guidance to facilitate study start-up and execution while maintaining legal compliance.
- Clinical Contract Associate (CCA) Team oversight: Co-lead with the head of function, the recruitment process for the CCA team (workforce planning, job descriptions, interviews, selection, and onboarding). Define, deploy, and continuously improve the onboarding and training program to ensure consistent understanding of clinical contracting processes, compliance requirements, and internal SOPs.
Qualifications:
- Master's degree in Law (mandatory)
- Proven experience in clinical contract negotiation and/or data privacy compliance within the pharmaceutical, biotechnology, or CRO industry
- Prior experience working within the pharmaceutical industry.
- Strong working knowledge of GDPR, data protection regulations in clinical research, and clinical contracting frameworks
- Solid expertise in data protection and data privacy
- Fluent in English (written and spoken); French is a plus
Summary Location: Paris; London (UK) Type: Full time
Clinical Contract Manager in London employer: Ipsen
Ipsen Biopharm Ltd is an exceptional employer that prioritises a human-centric workplace culture, fostering collaboration and excellence. With a commitment to employee growth, Ipsen offers opportunities for continuous improvement and innovation in the biopharmaceutical field, particularly in vibrant locations like Paris and London. Employees are empowered to thrive, making a meaningful impact on patients and society while enjoying a supportive environment that values diverse perspectives.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Contract Manager in London
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Ipsen.
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We think you need these skills to ace Clinical Contract Manager in London
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 Ipsen!
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 Ipsen 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 Ipsen!
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 Ipsen, 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 Ipsen
✨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 Ipsen 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 Ipsen’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.
