We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide. The Associate Clinical Research Specialist oversees, designs, plans, and develops clinical evaluation research studies. This will be a remote position in Bogotá. Responsibilities may include the following, and other duties may be assigned: Oversee, design, plan, and develop clinical evaluation research studies Prepare and author protocols and patient record forms Conduct registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential Oversee and interpret results of clinical investigations in preparation for new drug, device, or consumer application Oversee and resolve 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 Responsible for clinical supply operations, site and vendor selection People working within the region/country may also have responsibilities that include: Represent Medtronic in clinical research within the country/region and collect feedback from local customers and authorities Build and maintain optimal relationships and effective collaborations with various internal and external parties Drive local evidence dissemination & awareness Required Knowledge and Experience: Bachelor's degree in Life Science Fluent in English One year of experience working with clinical research, regulatory affairs, or administrative areas Research experience in an academic space Knowledge of MS Office (Outlook, Word, Excel, PowerPoint) Knowledge of SAP is advantageous #J-18808-Ljbffr