Job Description
About the position Responsibilities • Oversees the conduct of clinical evaluation research studies with a primary focus on clinical site management. • Supports preparation of protocols and patient record forms. • Conducts registered and non-registered clinical studies of products satisfying a medical need and offering commercial potential. • Oversees and interprets results of clinical investigations in preparation for new drug devices or consumer applications. • Resolves operational aspects of clinical trials in conjunction with project teams under SOP, GCP, and specific country regulations. • May prepare clinical trial budgets and manage clinical supply operations. • Responsible for site and vendor selection. • Represents Medtronic from clinical research within the country/region and collects feedback from local customers and authorities. • Builds and maintains optimal relationships and effective collaborations with various internal and external parties. Requirements • Baccalaureate degree in engineering, life sciences, or related medical/scientific field. • Minimum of 4 years of clinical research experience or advanced degree with a minimum of 2 years experience. Nice-to-haves • 5+ years' experience managing clinical trials within Medtronic or medical device industry. • Experience managing multiple clinical research sites with proven results in study execution. • Experience in managing clinical trial data review. • Basic understanding of biostatistics and trial design. • Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials, such as CFR 812, 50, 54, and ISO14155:2020. • Experience in Pain management therapies/products. Benefits • Competitive salary and flexible benefits package. • Short-term incentive called the Medtronic Incentive Plan (MIP). • Wide range of benefits, resources, and competitive compensation plans designed to support employees at every career and life stage. Apply tot his job