Field Clinical Research Specialist, 7-Month Fixed-Term Contract

🔥 17 hours ago

🇫🇷 France – Remote

💵 €46k - €69k / year

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Medtronic

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1949

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

Healthcare • Manufacturing • Healthcare Insurance

Medtronic is a global leader in healthcare technology solutions, working to address the most complex and challenging medical conditions. With over 95,000 employees in more than 150 countries, the company is focused on accelerating access to healthcare technologies and advancing inclusion, diversity, and equity in healthcare. Medtronic collaborates closely with healthcare professionals to innovate and optimize treatments and therapies, thus inspiring hope and new possibilities for patients worldwide. The company's commitment to healthcare extends to its focus on impactful solutions and sustainable practices.

📋 Description

• Ensure the implementation and operational follow-up of pre- and post-market clinical studies • Identify, select, and support investigators and participating sites throughout the study lifecycle • Organize and conduct investigator site training, activation, monitoring, and close-out activities • Ensure compliance with study protocols, Good Clinical Practice (ICH-GCP), and applicable regulatory requirements • Support sites with patient recruitment and follow-up to optimize enrollment and the quality of collected data • Participate in initial implant procedures and selected study visits to support data collection and the proper execution of study protocols • Build and maintain trusted relationships with investigators, research teams, and key hospital stakeholders • Serve as the primary point of contact for investigator sites regarding Medtronic EPT clinical studies • Collaborate with international clinical research teams and cross-functional stakeholders to contribute to study success • Share field insights and contribute to the continuous improvement of clinical research protocols, tools, and processes

🎯 Requirements

• Master’s degree or equivalent qualification in clinical research, life sciences, or biomedical sciences • At least 4 years of experience in clinical research, ideally within the medical device industry • Experience managing clinical studies and/or monitoring investigator sites • Strong knowledge of Good Clinical Practice (ICH-GCP) and applicable regulatory requirements for clinical trials • Experience collaborating with healthcare professionals, investigators, hospital teams, and internal partners • Excellent interpersonal and communication skills • Self-motivated, well-organized, and able to manage multiple projects simultaneously • Proactive, with a strong results orientation • Ability to work in an international matrix environment • Fluency in French and English, both written and spoken • Frequent travel throughout France (up to 60% of the time)

🏖️ Benefits

• Competitive salary and flexible benefits package • Wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage • Short-term incentive called the Medtronic Incentive Plan (MIP)