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Early Clinical Phase Project Manager, 12M
- International environment and chance to improve your English
- Competitive salary and flexible working arrangements
About Our Client
Do you want to be a part of a global top 10 CRO? This company is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of the company in 1998, to where we are today, we've continued to improve what we do.
We are currently looking to strengthen our Clinical Project Management team in Japan and are seeking a Clinical Project Manager for Early Phase Development to be based in Tokyo or Osaka office.
Provides customer-focused leadership in managing clinical trials across various phases and functional areas and assigned clinical staff. Accountable for the successful execution of all assigned projects, where success includes on-time, on-budget, high quality/compliant project results that lead to satisfied customers. Acts as an integral part of the selling team through involvement in proposal development and bid defense. Serves as the primary liaison with Customers, vendors, and Investigator Sites. May have line management responsibility for assigned clinical staff. Manages projects from proposal development to final deliverables to the customer ranging in size and complexity from single service studies to full scope, multiple protocol projects, which may be global, with limited interaction from supervisor.
The Successful Applicant
BA/BS in the life sciences, nursing degree, or equivalent combination of education and experience. Moderate clinical research experience in a contract research organization, pharmaceutical, or biotechnology company. Clinical research organization (CRO) and relevant therapeutic experience preferred. Previous technical and managerial experience in conducting multi-national and/or local clinical trials in a hospital setting, pharmaceutical company, or CRO preferred. Thorough knowledge of regulatory requirements, drug development, and clinical monitoring procedures. Demonstrated proficiency with ICH/GCP guidelines. Keen insight, independent judgment, and tactful discretion. Presentation, documentation, and interpersonal skills as well as a business communication language skills in both Japanese and English. Proficient computer skills in Word, Excel, PowerPoint, email and Internet. Basic computer skills using MS Project. Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
What's on Offer