Albuquerque, NM30+ days ago
Assist with the informed consent process with care and quality • Adhere to study protocol and GCP • Provide high quality source data capture and documentation • Supporting the IP distribution and accountability process • Adverse Event tracking and follow-up • Data entry to CRF/EDC and query resolution • Protocol deviation tracking, reporting, and reconciliation • Attending sponsor visits including SIVs, IMVs, and COVs, as needed • Use and help improve Topography's proprietary tool set. Act as research assistant to clinical trials conducted within physician practices, including but not limited to: • Visit preparation activities • Visit follow-up activities • Supply and inventory coordination • Third party vendor coordination • Patient recruitment and identification • Assist with patient study visits • Assist with clinical and lab procedures such as ECG, phlebotomy, vitals signs and body measurements, laboratory processing, etc.