北京招聘

职位描述：
Position Summary:
Be responsible for planning, implementation and daily handlings of shipment orders to ensure clinical trial materials are well- supplied in accordance with the cGMP standards.


Key Responsibilities:
1.Perform all processes in accordance to established procedures and cGMP standards
2.Support the activities of planning, implementing, motivating, co-monitoring, and tracking study documents and tracking tools
3.Coordinate to ensure the shipment orders processing in a timely and accurate manner in accordance with cGMP standards
4.Confirmation of previously entered data and completion of data entry
5.Complete regular reports (as required by Management or client) pertaining to relevant work areas
6.Support PM to update contact listings, update checklist, generate and compile reports as requested.
7.Other job assigned by supervisor

Minimum Requirements/Qualifications:
Education: college diploma above
Years of Experience: 1-2 yrs relevant working experience. Experience in freight operation, logistics management or international trade.
Knowledge: Logistics, international trade.
Competency: Good command of English; good command of MS office application; communication and coordination skills; customer-oriented.

Non-Negotiable Hiring Criteria:
1.College diploma holder
2.Communication and coordination skills
3.Customer – oriented 举报 分享

Fisher Clinical Services is a part of the CTD of Thermo Fisher Scientific, the world leader in serving science, enabling our customers to make the world healthier, cleaner and safer. With annual revenues of $10 billion, we have more than 30,000 employees and serve over 350,000 customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as environmental and industrial process control settings.