General Information

Location: Tokyo, Japan

Organization: Medavante-Prophase, Inc.

Job Type: Full Time - Regular

Description and Requirements

The Project Associate provides project support to site management teams according to MedAvante-ProPhase’s Standard Operating Procedures (SOPs) and Good Clinical Practices (GCP). The Project Associate will be responsible for shipping and receiving for the office that they are based in. 

EDUCATION REQUIREMENTS: 
  • Associate degree (or local equivalent) preferred, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or the equivalent combination of education, skills and experience to perform the job. 

QUALIFICATIONS/EXPERIENCE: 
  • Ability to work in a fast-paced environment and support multiple projects concurrently and able to manage a variety of tasks. 
  • Ability to work within a project team. 
  • Good planning, organization and problem-solving abilities. 
  • Able to quickly and accurately type and enter data. 
  • Effective communication skills, oral and written. 
  • Proficient in MS Office, specifically Word, Excel and Outlook. 
  • Ability to create spreadsheets with large numbers of figures without mistakes. 
  • Formal computer training is preferred. 
  • Strong attention to detail. 
  • Must be proficient in Japanese and English. Other languages are a plus. 
  • Ability to work flexible hours to provide support on a global basis as needed. 

ESSENTIAL DUTIES/RESPONSIBILITIES: 
  • Assist site management teams with project implementation by ensuring that all systems are configured, maintained and updated with the appropriate site information. 
  • Provide timely and accurate status reports to internal and external key stakeholders. 
  • Initiate site shipping requests and prepare packages for shipment in a timely manner ensuring the correct information is provided. 
  • Needs to be able to pack and move packages up to 25 lbs. 
  • Correct and modify inaccurate data and records. 
  • QC site source documents for accuracy. 
  • Retrieve data from the database or electronic files as requested. 
  • May serve as the office administrator/receptionist
ABOUT US:
MedAvante-ProPhase, a subsidiary of WIRB-Copernicus Group (WCG) was founded in 2002 with the goal of helping to bring better drug therapies to market through smarter, faster clinical trials. With this goal in mind, MedAvante - ProPhase  set out to solve one of Pharma’s most intractable problems: the bias and variability that cause failed or inconclusive trials for Central Nervous System (CNS) therapies. A few years later, MedAvante - ProPhase  experts pioneered Central Ratings and introduced the concept of Central Review utilizing their groundbreaking Virgil eSource solution.