上海招聘

Role and your Responsibilities:
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies ensuring that applicable regulations and principles of ICG-GCP are adhered to.

Additional Responsibilities:
? Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
? Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
? Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
? Managing queries efficiently and responsible for study cost effectiveness

What is Required
With a University degree in medicine, science, or equivalent, you will have previous monitoring experience in medium sized studies including study start up and close out. In addition, you will also require:

? You will have knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
? Fluent in English as well as the local language
? Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
? Ability to produce accurate work to tight deadlines within a pressurized environment
? Computer literate with Microsoft Office
? Must be available to travel.

What is Offered?
You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.


For further information about this position contact:
Jackie.xu@docsglobal.com

A global leading company focus on the drug research, clinical research and providing Clinincal operation solution for world famous pharamcy company. We have over 9000 people all of the World and entered into China in 2005. Will with a good development plan to broaden and improve China business scale.