CRA II

Full work from home CRA

Your new company
A global midsize CRO/ Clinical Trials

Your new role
  • Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
  • Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
  • Actively participate in study team and investigator meetings
  • Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)


What you'll need to succeed
  • Step up up from CRA
  • Work closely with global
  • Full work from home


What you'll get in return
  • Four-year college curriculum in life sciences, OR
  • Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.g. study coordinator, CTA, etc.)
  • Ability to meet the travel requirements of the job


What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV to riku.shionoya@hays.co.jp, or call 0335602890 now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1088743

Summary

Job Type
Permanent
Industry
Healthcare & Medical
Location
Inner Tokyo
Specialism
Life Sciences
Ref:
1088743

Talk to a consultant

Talk to Riku Shionoya, the specialist consultant managing this position, located in Tokyo Head Office
Izumi Garden Tower 28th Floor, 1-6-1 Roppongi

Telephone: 0335602890