Research Team Recruiter
Core
Recruit subject volunteers for Phase I clinical research studies and conduct Informed Consent sessions.
Role type
Clinical research coordinator / study screener
Builds
Clinical trial screening processes and subject enrollment
Domain
Clinical research / Pharmaceutical trials
Deliverable
physical/clinical work
Required skills
Informed consent administration, study protocol review, screening logistics, regulatory documentation (FDA), clinical lab review coordination, volunteer management
Preferred skills
Ability to administer investigational drugs or devices, experience in clinical environments
Technologies
Computerized phone-screening tools, clinical lab systems
Responsibilities
Review protocols for inclusion/exclusion criteria, set up participant screenings, conduct Informed Consent sessions, ensure proper consent and paperwork completion, coordinate physician reviews of clinical labs and ECGs, develop screening tools and source documents