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Clinical Research Monitor (CRA) (m/f/d)
Clinical Research Monitor (CRA) (m/f/d)-February 2024
Meerbusch
Feb 11, 2026
About Clinical Research Monitor (CRA) (m/f/d)

  Careers that Change Lives

  Join a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. This is a fantastic opportunity to be part of cutting-edge clinical research for medical devices. Come strengthen your specialized skills and enhance your expertise. We’ll support you with the training, mentorship, guidance, and networks you need to advance, and empower you to work in the way that’s best for you. Together, we can confront the challenges that will change the face of healthcare. Join us for a career that changes lives.

  As the Clinical Research Monitor you would be responsible for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory standards, Ethics Committee/Institutional Review Board (IRB/EC) policies as well as procedures and business policies. This position works under supervision as needed, with a lot of flexibility for personal development. You would work closely with study management teams within Medtronic and site personnel for resolution of site issues towards successful clinical studies execution.

  A Day in The Life

  Training investigators and site personnel.

  Performing monitoring activities of clinical trials at the site or remotely and ensuring all is conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.

  Collaborating with clinical investigators, affiliated hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug or medical devices approval.

  Reviewing adverse event cases with investigators, preparing study documents, and issuing reports.

  Recommending qualified investigators for sites selection.

  You may be assisting with design and monitoring planning of clinical evaluation projects.

  Must Haves

  You have a Bachelor or Master’s degree in life sciences, nursing or other health related disciplines or comparable qualifications

  You have experience in Clinical Research related activities

  You have at least 1 year experiences of Clinical Research Monitoring

  You have a basic understanding of any applicable regulations and standards (e.g., Training on Good Clinical Practices, ICH (International Council for Harmonisation) guidelines, FDA CFR (Code of Federal Regulations of the Food and Drug Administration), ISO 14155, clinical research ethics, EU Directive, etc.)

  You are Fluent in German and English

  You are eager to learn, talented, dynamic, motivated, passioned & team-player

  Nice to Haves

  Business knowledge or experience with the medical device industry

  Experience working with Word, PowerPoint, Excel spreadsheets and databases applications

  Language skills in French or Dutch are a strong advantage

  We Offer

  We offer a competitive salary and benefits package to all our employees:

  Flexible working environment

  Annual Incentive Plan % depending on company results

  Pension scheme and group discount on healthcare insurance

  Training possibilities via Cornerstone/Skills Lab

  Employee Assistance Program and Recognize! (our global recognition program)

  Our Commitment

  Our unwavering commitment to inclusion, diversity, and equity (ID&E) means zero barriers to opportunity within Medtronic and a culture where all employees belong, are respected, and feel valued for who they are and the life experiences they contribute. We know equity starts beyond our workplace, and we must play a role in addressing systemic inequities in our communities if we hope to have long-term sustainable impact. Anchored in our Mission, we continue to drive ID&E forward both to enhance the well-being of Medtronic employees and to accelerate innovation that brings our lifesaving technologies to more people in more places around the world.

  About Medtronic

  Bold thinking. Bolder actions. We are Medtronic.

  We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world.

  In everything we do, we are engineering the extraordinary .

  Your Answer

  Is this the position you were waiting for? Then please apply directly via the apply button!

  #LI-Remote

  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.

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