Entry-Level Contract Specialist, 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 Contract Specialist, Study Start-Up to join our Clinical Operations team in Japan. This position plays a key role in the study start-up and clinical trial management processes at Medpace.  The Site Contract Specialist will play a key role in advancing the start-up of our projects.  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; Hybrid work style and adaptable working hours; Annual company bonus; Annual merit salary increases; Defined Contribution Plan; Group term life insurance; Insurance association benefits available; Clear pathways for career growth, with opportunities to step into leadership roles; Collaboration with a diverse, international team and gain global exposure; Many additional perks unmatched by other CROs!

Serve as a liaison between Sponsor, investigative sites and Medpace; Negotiate contracts and budgets with investigative sites; and Collaborate with internal project team to ensure negotiations occur within timelines.

Bachelor’s degree or Juris Doctorate/Advanced degree within the field of law; Knowledge of clinical trials, preparation and maintenance of contracts and budgets; Strong attention to detail and excellent communication skills. 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