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
Responsibilities
- 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.
Qualifications
- 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.
- Bilingual Japanese and English
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,900 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Tokyo MedpaceWe are currently seeking new grads for full-time Contract Specialist position in Japan. This role plays a key role in the study start-up and clinical trial management processes at Medpace. · Serve as a liaison between Sponsor, investigative sites and Medpace; · Negotiate contract ...
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Tokyo MedpaceWe are seeking a full-time Contract Specialist to join our Study-Start-Up team in Tokyo. · Serve as a liaison between the Sponsor, investigative sites and Medpace; · Negotiate contracts and budgets with investigative sites; and · Collaborate with internal project team to ensure n ...
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