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Senior Clinical Research Associate - Oncology
ICON
East Coast
About this role
Senior Clinical Research Associate - Oncology - East Coast
What you will be doing:
- Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines.
- Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites.
- Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB/IEC submission support, and budgets and contracts negotiations.
- Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
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