Five 5 years of experience with ICH and GCP guidelines; and One or more clinical trial lifecycle areas, startup, enrollment, database locks, vendor management and closeout, health authority inspections, final clinical study reports, or TME reconciliation. Two 2 years of experience with Therapeutic area knowledge such as CNS, Oncology, Infectious Disease, Vaccine, or General Medicine and clinical development guidelines and directives. One 1 year of experience with Leading global trials.br br br Minimum Education and Experience Bachelors degree in Biology, Life Sciences, Genetics, Pharmaceutical Science, Pharmacology, or related field, and eight 8 years of experience as a Clinical Research Associate, Clinical Operations Manager, Study Manager, Clinical Project Manager, Research Associate, or related role.

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