Entry Level Regulatory Submissions Coordinator, Tokyo

Looking for Immediate Starters as well as 2027 Starters. We have mutiple Onboarding Batches to accomodate to your graduation date/current situation.   Our clinical operations activities are growing rapidly, and we are currently seeking new grads for full-time, office-based Regulatory Submissions Coordinator to join our Site Activation & Maintenance team in Tokyo, Japan. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.   We offer the following:  - Customized training program; - Annual company bonus; - Annual merit salary increases; - Defined Contribution Plan; - Group term life insurance; - Insurance association benefits available; - The opportunity to work from home; - Flexible work hours across days within a month; - Opportunity for leadership positions/career advancement; - Opportunities to work with international team; - Many additional perks unmatched by other CROs! Responsibilities - Quality check on submission documents and site essential documents; - Interaction with US Central IRBs, sites and international associates; - Preparation and approval of informed consent forms; and - Review pertinent regulations to develop proactive solutions to start-up issues and challenges. Qualifications - A Bachelor's degree in a relevant field, or Master's degree within Life Sciences; - Knowledge of local regulations regarding clinical studies and the conduct of such studies; - Strong communication skills; - Excellent computer skills, including a working knowledge of Microsoft Office applications. - Native level Japanese (JLPT N1) is standard, a minimum English TOEIC score of 500 or equivalent. Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace? When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.   Purpose-Driven Work - - Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence   Collaborative Culture - - Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. - Leadership throughout Medpace is both accessible and approachable   Continuous Growth & Development - - Office based environment with on-site mentors - Defined career paths with clear advancement opportunities - Industry renowned onboarding and training programs designed to accelerate professional development - Ongoing training and continuous learning opportunities throughout your career - An environment that encourages employees to influence change, contribute ideas, and grow quickly   Other Employee Benefits - - Competitive compensation programs that recognize and reward performance - Comprehensive health, wellness, retirement, and PTO benefits - Office based culture with occasional WFH that provides flexibility for eligible positions after training - Company-sponsored social events    Please note benefits may vary based on country.      What to Expect Next A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted. - Quality check on submission documents and site essential documents; - Interaction with US Central IRBs, sites and international associates; - Preparation and approval of informed consent forms; and - Review pertinent regulations to develop proactive solutions to start-up issues and challenges. - A Bachelor's degree in a relevant field, or Master's degree within Life Sciences; - Knowledge of local regulations regarding clinical studies and the conduct of such studies; - Strong communication skills; - Excellent computer skills, including a working knowledge of Microsoft Office applications. - Native level Japanese (JLPT N1) is standard, a minimum English TOEIC score of 500 or equivalent.