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