Job Description
My client is looking for two drug safety associates to join their team in the South East. You will be responsible for monitoring, reporting adverse events and serious adverse events for clinical studies.
Ideally you will be a self motivated person who can work independently. You will have the ability to be self sufficient and able to conduct all procedures in relation to safety monitoring.
Responsibilities will include:-
Familiarity with SOP's, reporting SOP's and other appropriate regulations.
Good communication skills in order to
Maintenance of adverse event database, tracking system and paper files.
for more information please call Zoe on 01580 201616 or email zoe.bennett@bluepelicanpharma.com
Qualifications/Skills Required
Drug safety, clinical research, clinical data
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