Senior Clinical Research Specialist

Medtronic, City of Westminster

Senior Clinical Research Specialist

Salary not available. View on company website.

Medtronic, City of Westminster

  • Full time
  • Permanent
  • Remote working

Posted 1 day ago, 24 Aug | Get your application in today.

Closing date: Closing date not specified

Job ref: edbba0be59b24c60a00f8112ba33248e

Location ref: City of Westminster

Full Job Description

The Senior Clinical Research Specialist manages Investigator Sponsored Research (ISR) studies, provides clinical documentation support to the ISR program, and leads continuous improvement of related processes and logistics. This role supports all Surgical business units and operates within a global team, requiring flexibility across global time zones. The role requires a high degree of professionalism, sound judgment, and integrity in all interactions, particularly as it requires engaging with healthcare professionals (HCPs), investigators, and external research partners. In this exciting role as a Sr Clinical Research Specialist (CRS) in our Surgical Operating Unit (OU), you will manage Investigator-Sponsored Research (ISR) studies, provide clinical documentation support, and lead continuous improvement across ISR processes and logistics. Operating within a global team, this role supports all Surgical business units and requires flexibility across time zones, alongside a high degree of professionalism, sound judgment, and integrity when engaging with healthcare professionals (HCPs), investigators, and external research partners. Most of your time will be spent driving the operational execution, financial administration, and oversight of ISR studies-from review and contract negotiation through close-out and publication. You will work with centralized internal teams and global stakeholders to maintain Trial Master Files (TMF), ensure GCP and regulatory compliance, and optimize workflows spanning payments, device logistics, and GCC approvals. Our Surgical OU brings together three Business Units to deliver high-quality clinical evidence from concept to commercialization. As part of this dynamic environment, you will also serve as a Subject Matter Expert for clinical and purchasing systems, support Medtronic-sponsored study activities, and act as the European representative on the global ISR Council of Expertise. Responsibilities may include the following and other duties may be assigned:

  • End-to-End ISR Management: Oversee investigator-sponsored research from initial review, contracting, and active study management through close-out and publication.
  • Device & Logistics Execution: Manage study device shipments, returns, and associated logistics for assigned studies.
  • Financial Administration: Handle ISR costing, budgeting, invoicing, payment processing, and asset depreciation tracking.
  • Contracting & Stakeholder Alignment: Coordinate contract negotiations and align internal cross-functional stakeholders to ensure timely execution.
  • Quality & Audit Readiness: Maintain Trial Master Files (TMF) and ensure compliance with GCP, ISO 14155, regulatory requirements, and internal SOPs.
  • Global Representation & Policy Support: Serve as the European representative on the global ISR Council of Expertise and help develop/update study policies and procedures.
  • Sponsor Study Support: Assist Medtronic-sponsored studies with payments, budget management, and Global Compliance Committee (GCC) approval workflows.
  • Systems & Process SME: Act as Subject Matter Expert for purchasing systems, clinical trial management platforms, HCP interactions, and operational workflows.
  • Process Improvement: Lead initiatives to optimize contracting, payment, device logistics, and compliance approval processes.
  • Cross-Functional Collaboration: Partner closely with internal teams and present key updates during Medical Evidence team meetings.

    Bachelor's degree with 4+ years of clinical research experience, or an advanced degree with 2+ years of clinical research experience.
  • 5+ years of experience managing or supporting clinical trials within the medical device industry, including experience working on European pre-market studies and managing multiple clinical research sites.
  • Strong knowledge of Good Clinical Practice (GCP), clinical trial regulations, and relevant standards (e.g., CFR 812, CFR 50, CFR 54, ISO 14155).
  • Fluent in English, with excellent written and verbal communication skills.
  • Proven ability to manage multiple priorities independently and collaborate effectively within cross-functional teams.
  • Strong problem-solving, organizational, and project management skills, with high attention to detail.
  • Professional and compliant stakeholder management skills, including effective interactions with healthcare professionals (HCPs), investigators, and internal teams.
  • Willingness and ability to travel up to 20%.
  • Preferred Qualifications : Experience building and maintaining scientific literature databases+ Experience with payment processes, contracting, and HCP engagement activities.

    Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact., Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
  • We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. We change lives . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives. We build extraordinary solutions as one team . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough. This life-changing career is yours to engineer . By bringing your ambitious ideas, unique perspective and contributions, you will…
  • Build a better future, amplifying your impact on the causes that matter to you and the world
  • Grow a career reflective of your passion and abilities
  • Connect to a dynamic and inclusive culture that welcomes the challenge of life-long learning
  • These commitments set our team apart from the rest: Experiences that put people first . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need. Life-transforming technologies . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms. Better outcomes for our world . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls. Insight-driven care . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.

    Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 60,800.00 EUR - 91,200.00 EUR | United Kingdom: 50,400.00 GBP - 75,600.00 GBP | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Direct job link

https://www.jobs24.co.uk/job/senior-clinical-research-specialist-127250619
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