Conducts monitoring activities of assigned clinical trials in compliance with the protocol, ICH-GCP/ISO14155 and all applicable local laws and regulations, company policies and quality standards. Performs management of study site activities to ensure the collection of accurate clinical data within given timelines. May be responsible for multiple studies and must work independently with team support. Position can be regional or office based.
PRIMARY JOB FUNCTIONS:
Manages all ...
Premier Research Group Limited - 18 months ago
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