Clinical Research Associate - Remote - Oncology - (Apex, NC)

Overview Candidates must have Oncology monitoring background to be considered. The Clinical Research Associate is responsible for the monitoring of clinical trials and tracking of study progress, thereby contributing to the overall management of clinical trials in accordance with the appropriate quality standards including ICH-GCP guidelines, Standard Operating Procedures (SOPs), applicable regulations, rules and guidance. S/he is responsible for clinical site start-up, maintenance, and closure activities, including maintenance of study documents. This role may be located remote Anywhere, US. Responsibilities Interfaces with study team to ensure timely initiation and completion of clinical trials Responsible for the identification, evaluation and qualification of investigators and sites May prepare and submit essential document packages to clinical sites required for clinical site initiation.