Senior Clinical Study Manager

ABOUT INSPIRE MEDICAL SYSTEMS Inspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Inspire Medical Systems is committed to enhancing patients’ lives through sleep innovation. We are steadfast in our commitment to prioritize patient outcomes, act with integrity and lead with respect. With positive persistence at our core, we are committed to all those we serve. WHY JOIN OUR FAST-GROWING TEAM At Inspire, we value people – your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people-first culture by offering excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement. If you’re passionate about making a difference in people’s lives and want to work with innovative technology, come be a part of our great team! POSITION SUMMARY This position is for overseeing clinical activities related to one or more clinical studies and performing/managing the daily in-house operations associated with the studies. The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may have direct reports. MAIN DUTIES/RESPONSIBILITIES Responsible for managing clinical studies in accordance with internal standard operating procedures and applicable regulations and guidelines Collaborate with internal and external clinical team members, consultants and/or CROs to draft clinical study protocols and other clinical study documentation Oversee clinical site selection and activation Manage study safety by tracking and reporting adverse events as required by regulatory bodies, reviewing adverse event trends, and overseeing safety committees including Clinical Events Committees and Data Safety Monitoring Boards Oversee monitoring activities related to assigned clinical studies including review and approval of monitoring plan and monitoring reports, managing monitoring schedule and ensuring corrective action related to monitoring findings Develop training plans for study training and review/approve training documentation Prepare study-related reports including annual, interim and final study reports Organize and lead study-related conference calls and Investigator meetings as needed through the study Oversee investigational device allocation, distribution and reconciliation Collaborate with data management team and/or CRO to ensure appropriate data capture, query management and to identify data analysis needs Use critical thinking skills to review and analyze scientific journal articles Assist with generation and/or review of study-related abstracts, posters, presentations, manuscripts as needed QUALITY SYSTEM RESPONSIBILITIES Document product and therapy related field reports within the prescribed timelines and provide any necessary documents required to complete the investigation. Provide follow-up reporting as needed. Complete training requirements and competency confirmations as required for this position within the required timeline. Comply with applicable quality system procedures/policies and make suggestions for continuous process improvement. Ensure all direct reports maintain training records that comply with applicable quality system requirements. (if applicable) QUALIFICATIONS Educational Requirements: Required: Bachelor’s Degree required Preferred: Science Degree preferred (Biology, Chemistry, etc.) Required Experience: Previous clinical research experience (minimum 5 years) required Previous clinical study management experience preferred International clinical experience preferred Previous collaborat…