Clinical Research Monitor – CRA

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Medtronic

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1949

⚕️ Healthcare Insurance

Healthcare Insurance • Medical Devices

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

• Responsible for monitoring activities and site management for clinical study • Oversees study sites and manage study investigators and study coordinators • Execute clinical study from study design to CSR report out • Oversees IRB submission/approval process • Oversees CTA agreement/amendment/ payment process • Oversees and interpret results of clinical investigations in preparation for new device • Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets • May be responsible for clinical supply operations, site and vendor management • Represents Medtronic from a clinical research respective within the country / region and also collects feedback from local customers and authorities • Builds and maintains optimal relationships and effective collaborations with various internal and external parties • Drives local evidence generation

🎯 Requirements

• Requires a Bachelor degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience • Excellent communication skills and stakeholder relationship management • Strong ability to work well within a team and autonomously • Computer skills (excellent knowledge of MS Office products) • Good prioritization and organizational skills • Natural problem-solver with a high attention to detail and accuracy • Experience in medical devices or pharmaceutical Industry

🏖️ Benefits

• Competitive Salary and flexible Benefits Package • Health insurance • Retirement plans • Paid time off • Professional development • Short-term incentive called the Medtronic Incentive Plan (MIP)