Driven Clinical Research Coordinator well-versed in study protocols, standard operating procedures, and general trial and research study oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 5 years of related experience to a challenging new role.
Collaborating with outside institutions to provide biospecimens and deidentified data
Manage proper PHI and deidentification procedures
Observing proper protocols when consenting patients to studies
Abstract data and follow longitudinally
Skilled in Access, Microsoft Office, FDA and IRB regulations