Research Specialist II - FT - Days - MCI
Core
Conducts Phase 1-4 clinical trials for patients, capturing study data and monitoring patient care and treatment side effects.
Role type
Clinical Research Specialist (Phase 1-4 Trials)
Builds
Clinical trial data and patient care coordination for pharmaceutical sponsors
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial monitoring, patient screening and consent, data documentation, regulatory compliance, adverse event reporting, specimen processing, multidisciplinary team coordination
Preferred skills
None stated
Technologies
EPIC
Responsibilities
Obtain medical history, monitor patient care and treatment side effects, document patient/study results, coordinate multidisciplinary team activities, conduct initiation/monitoring/close-out visits with sponsors, screen and consent patients using GCP guidelines, report adverse events, resolve data queries, process and ship study specimens
Seniority
Mid-level, hands-on IC
