Clinical Research Associate - 2024/2025 New Graduate for Osaka

Clinical Research Associate (CRA) for Osaka- join our growing team!

Are you a recent or upcomingnew graduate? We are seeking exceptional candidates that are passionate about healthcare and research. If you looking for a dynamic and rewarding career, you belong at Medpace. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work. Our CRA Training Program, PACE^® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.

We are looking for 2024‐2025 New Graduates with degrees in:

• Pharmacy
• Biology
• Biomedical Science
• Chemistry
• Healthcare Administration
• Nursing
• Pharmacology
• Medical/Clinical Laboratory Science
• Life Science

WE OFFER THE FOLLOWING:

• Customized training program based on your experience and therapeutic background and interest;
• Competitive travel bonus;
• Annual merit increases;
• The opportunity to work from home;
• Flexible work hours across days within a month;
• Laptop, mobile phone with hotspot for internet access anywhere and home office furniture allowance for home-based CRAs;
• Opportunity for leadership positions/career advancement – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager;
• User friendly CTMS with electronic submission and approval of monitoring visit reports;
• Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
• In-house administrative support for all levels of CRAs;
• Opportunities to work with international team of CRAs; and
• Many additional perks unmatched by other CROs!

• Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirement(s);
• Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to Medpace/Sponsor Standard Operating Procedures (SOPs);
• Serve as the primary resource to the clinical investigator and site staff;
• Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-functional teams;

• Native level Japanese and excellent reading and writing English skills
• Must have a minimum of a bachelor’s degree in a health or science related field;
• Ability to travel 60-80%/month to locations nationwide is required;
• Proficient knowledge of Microsoft^® Office;
• Strong communication and presentation skills; and