What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.
We are partnered with a growing company that is seeking a Senior Clinical Research Associate. The Senior Clinical Research Associate is responsible for the overall management and oversight of assigned clinical trial sites, including site identification, feasibility assessments,