Research Team Recruiter
Core
Recruit subject volunteers for Phase I clinical research studies and conduct Informed Consent sessions.
Role type
Clinical research coordinator / study recruitment specialist
Builds
Clinical trial screening processes and subject enrollment for pharmaceutical/biotech studies
Domain
Clinical research / Pharmaceutical trials
Deliverable
physical/clinical work
Required skills
Informed consent administration, study protocol review, screening logistics coordination, regulatory documentation (FDA), biohazard safety awareness, multi-tasking in clinical settings
Preferred skills
Ability to administer investigational drugs or devices, experience with clinical lab/ECG review workflows
Technologies
Computerized phone-screening tools, clinical lab requisition systems
Responsibilities
Conduct Informed Consent sessions with volunteers, prepare study paperwork and screening logs, coordinate screening schedules and physical exams, ensure regulatory compliance for subject data, review clinical labs and ECGs, develop screening tools and source documents
Seniority
Mid-level, hands-on operational role