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- Tasks: Manage clinical trial supplies and collaborate with cross-functional teams to ensure timely delivery.
- Company: Leading pharmaceutical company dedicated to innovative treatments and patient care.
- Benefits: Flexible working hours, hybrid model, and opportunities for professional growth.
- Why this job: Make a real difference in patients' lives while working in a dynamic and supportive environment.
- Qualifications: Pharmacist degree and 10 years of experience in Clinical Trial Supply Management.
- Other info: Join a passionate team on a mission towards a world free of pain.
The predicted salary is between 60000 - 80000 £ per year.
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What The Job Looks Like
- Being responsible for vendor relationship management and identifying potential external CTS service providers (e.g. Contract Manufacturing Organizations, Depots, Couriers, IRT providers).
- Being the central point of contact for all trial supplies related activities for all assigned trials/projects.
- Developing trial‑specific packaging concepts in alignment with relevant stakeholders to achieve packaging design which ensures proper handling by site staff/patients and fulfils any blinding requirements.
- Developing of trial‑specific supply strategy including depot involvement to ensure in‑time delivery of high quality clinical trial supplies.
- Coordinating and overseeing manufacturing tasks, e.g. planning, coordination of bulk manufacture, packaging and labelling, coordination of QP release, storage requirements.
- Overseeing outsourced tasks related to any aspect of clinical trial supplies management to ensure adequate performance, implementation of risk management and issues are identified/communicated and corrective actions implemented and documented appropriately.
- Maintaining and delivering budget oversight and forecasts.
What You'll Bring To The Table
- Pharmacist degree or comparable scientific, technical, or medical qualification.
- 10 years’ experience in Pharmaceutical Industry in field of Clinical Trial Supply Management, preferably CRO experience.
- Experience in budget forecast and budget tracking.
- Experienced in the conduct of clinical trials.
- Thorough understanding of applicable EU and US GMP regulations for IMP manufacturing.
- Thorough understanding of GDP requirements for setup of logistical part of supply chain and of GCP requirements in the conduct of Phase I – IV trials.
- Excellent analytical, organizational and communication skills.
- Service‑oriented mindset whilst enjoying working in interdisciplinary teams.
In this pivotal role, you will lead all aspects of clinical trial supply as part of a highly collaborative, cross‑functional team, working closely with internal teams and external vendors. Join us on our exciting journey towards a World Free of Pain.
Senior Clinical Supply Manager (m/f/d) in Maidenhead employer: Grünenthal Group
Contact Detail:
Grünenthal Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Supply Manager (m/f/d) in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience in clinical trial supply management. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in their mission of creating a world free of pain. Tailor your answers to reflect how your experience aligns with their goals.
✨Tip Number 3
Practice your pitch! You’ll want to clearly articulate your experience in clinical trial supply management and how it relates to the role. Keep it concise but impactful—think of it as your personal brand statement.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about joining our mission to change lives for the better.
We think you need these skills to ace Senior Clinical Supply Manager (m/f/d) in Maidenhead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Supply Manager role. Highlight your relevant experience in clinical trial supply management and any specific achievements that align with the job description. We want to see how you can make a difference!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for improving patients' lives and how your background fits with our mission. Be genuine and let us know why you’re excited about this opportunity.
Showcase Your Skills: Don’t forget to highlight your analytical, organisational, and communication skills in your application. These are key for the role, so give us examples of how you've used these skills in past experiences to tackle challenges.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Grünenthal Group
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial supply management and the specific regulations involved. Familiarise yourself with EU and US GMP regulations, as well as GDP requirements. This will not only show your expertise but also demonstrate your commitment to the role.
✨Showcase Your Experience
Prepare to discuss your past experiences in detail, especially those related to vendor management and budget oversight. Use specific examples to illustrate how you've successfully managed clinical trial supplies and navigated challenges in previous roles.
✨Ask Smart Questions
Come prepared with insightful questions about the company's current projects and future goals. This shows your genuine interest in the role and helps you understand how you can contribute to their mission of making a positive impact on patients' lives.
✨Demonstrate Team Spirit
Since this role involves working closely with cross-functional teams, be ready to discuss how you collaborate with others. Share examples of how you've worked effectively in interdisciplinary teams and highlight your service-oriented mindset.