At a Glance
- Tasks: Lead impactful clinical studies in pelvic health across Europe, shaping patient care.
- Company: Join Medtronic, a global leader in healthcare innovation.
- Benefits: Competitive salary, flexible benefits, and a supportive work environment.
- Other info: Opportunity for career growth in a diverse and inclusive company.
- Why this job: Make a real difference in healthcare while working remotely with a dynamic team.
- Qualifications: Experience in managing international clinical studies and strong communication skills required.
The predicted salary is between 64800 - 97200 € per year.
Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.
Journée type
We are seeking a Principal Clinical Research Specialist to serve as a Study Manager supporting Pelvic Health clinical studies across Europe, including the UK, France, Belgium, and Germany. This role offers the opportunity to lead and shape the execution of meaningful clinical research that directly impacts patient care. As a Study Manager, you will take ownership of multi-site studies from start‐up through close‐out, working closely with investigators, cross‐functional partners, and external vendors to deliver high‐quality, compliant clinical evidence in a dynamic, global environment. This is a remote position that will partner closely with the Pelvic Health clinical team based in Minneapolis, MN. Travel up to 20% is expected to support site engagement and study execution.
Responsibilities may include the following and other duties may be assigned:
- Lead the design, planning, and execution of registered and non‐registered Pelvic Health clinical studies, including authorship of clinical protocols, case report forms, and related study documents.
- Provide end‐to‐end operational oversight of multi‐site clinical trials, ensuring compliance with SOPs, GCP, and country‐specific regulations, and supporting clinical trial budget development as needed.
- Interpret and oversee clinical investigation data to support medical evidence generation, regulatory submissions, and new or expanded device applications.
- Manage key operational components of clinical studies, including clinical supply operations, site and vendor selection, and cross‐functional coordination with internal and external partners.
- Serve as a clinical research representative within the assigned region, building strong relationships with investigators, customers, and regulatory authorities, while driving local evidence dissemination and incorporating regional feedback into study execution.
Required Knowledge and Experience:
- Extensive experience managing multi‐site, international clinical studies within the medical device or regulated healthcare industry, with demonstrated Study Manager–level accountability.
- Strong working knowledge of ICH‐GCP, ISO 14155, EU MDR, UK clinical research requirements, and applicable country‐specific regulations, with hands‐on application in study execution.
- Prior experience authoring and reviewing clinical study documentation, including protocols, CRFs, and clinical reports, and interpreting clinical data to support evidence generation and regulatory needs.
- Demonstrated ability to manage clinical trial operations, including vendor and site oversight, clinical supplies, budgets, and cross‐functional collaboration in a global environment.
- Strong communication, stakeholder management, and organizational skills, with the ability to work independently in a remote role.
Avantages sociaux et rémunération
Medtronic offre un salaire compétitif et un ensemble d’avantages sociaux flexibles. Le cœur de nos valeurs est animé par un engagement envers nos employés. Nous saluons leurs contributions et partageons avec eux le succès qu’ils ont contribué à créer. Nous offrons un large éventail d’avantages, de ressources et de régimes de rémunération concurrentiels conçus pour vous soutenir à chaque étape de votre carrière et de votre vie personnelle.
Pay range: United Kingdom: 64,800.00 GBP - 97,200.00 GBP. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
À propos de Medtronic
Nous sommes à la pointe de la technologie mondiale en matière de soins de santé et nous nous attaquons avec audace aux problèmes de santé les plus difficiles auxquels l’humanité est confrontée en recherchant et en trouvant des solutions. Notre mission (soulager la douleur, restaurer la santé et prolonger la vie) rassemble une équipe mondiale de plus de 95 000 personnes passionnées. Nous sommes des ingénieurs dans l’âme et nous mettons en œuvre des idées ambitieuses pour trouver de véritables solutions pour des personnes bien réelles.
Spécialiste principal recherches cliniques in Watford employer: Medtronic plc
At Medtronic, we pride ourselves on being a leading global healthcare technology company that fosters a culture of innovation and collaboration. As a Principal Clinical Research Specialist based in Watford, you will enjoy a flexible remote work environment, competitive salary, and comprehensive benefits designed to support your professional growth and personal well-being. Join us in making a meaningful impact on patient care while working alongside passionate colleagues dedicated to advancing healthcare solutions.
StudySmarter Expert Advice🤫
We think this is how you could land Spécialiste principal recherches cliniques in Watford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for those interviews! Research Medtronic and understand their mission and values. Tailor your answers to show how your experience aligns with their goals, especially in Pelvic Health clinical studies.
✨Tip Number 3
Showcase your skills! Bring along examples of your previous work managing multi-site clinical trials. Be ready to discuss how you ensured compliance and delivered high-quality results, as this will impress the hiring team.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining the Medtronic team.
We think you need these skills to ace Spécialiste principal recherches cliniques in Watford
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Principal Clinical Research Specialist role. Highlight your relevant experience in managing multi-site clinical studies and your knowledge of ICH-GCP and EU MDR regulations. We want to see how you fit into our mission!
Showcase Your Skills:Don’t just list your skills; demonstrate them! Use specific examples from your past experiences that showcase your ability to lead clinical studies and manage cross-functional teams. This will help us understand how you can contribute to our dynamic environment.
Be Clear and Concise:When writing your application, keep it clear and to the point. Avoid jargon and make sure your key achievements stand out. We appreciate straightforward communication, so let’s keep it simple and effective!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to the right people. Plus, you’ll find all the details about the role and our company culture there!
How to prepare for a job interview at Medtronic plc
✨Know Your Stuff
Make sure you have a solid understanding of clinical research principles, especially ICH-GCP and ISO 14155. Brush up on the specifics of Pelvic Health studies and be ready to discuss how your experience aligns with the role.
✨Showcase Your Leadership Skills
As a Principal Clinical Research Specialist, you'll need to demonstrate your ability to lead multi-site studies. Prepare examples of past projects where you successfully managed teams and collaborated with cross-functional partners.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous studies and how you overcame them, particularly in a remote or international context.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and how they ensure compliance across different regions. This shows your genuine interest in the role and helps you gauge if it's the right fit for you.