Dispatched to a well-known 3A hospital to conduct international multi-center clinical
research for multinational pharmaceutical companies,and assisted the investigators to
complete various non-scientific judgments of clinical trials according to the
requirements of GCP and clinical programs.
Assist the investigators to choose and follow the subjects.
Assist the investigators to collect and manage the date.
Input the clinical trial data entry.
Major in clinical medicine,pharmacy,pharmaceutics or nursing, etc.
Good English Skills in both writing and speaking.
Strong ability in work independently and team spirit.
Certainly fit to work under pressure, and self-psychological adjustment.
Self-motivated, good communication and adaptability, good self-learning ability.
▪ PM (Project Manager)
Responsible for overseeing all aspects of CRC clinical study, controlling project
progress and quality.
Responsible for providing professional program and process training for CRC.
Manage the financial whereabouts of all members of the project team
Complete the project quotation and bidding documents and participate in client bidding.
Visit the customers regularly, collect the relevant feedback, and improve the service
Responsible for drafting and revising departmental SOP.
Major in pharmacy, nursing or medicine, etc.
At least 2 years CRC working experiences, 1 year personnel management experience is
Excellent communication and coordination skills.
Good team spirit, proactive and detail-oriented.
Strong ability to work under pressure and accept work overtime.