Research Engineering/Scientist Associate III
Core
Independently designs and conducts complex research projects, analyzes data, supervises junior staff, and manages participant recruitment and enrollment for clinical studies.
Role type
Senior Research Associate (Clinical Research & Operations)
Builds
Clinical research studies and data collection protocols
Domain
Women's Health / Clinical Research
Required skills
Participant recruitment and enrollment, Informed consent administration, Regulatory compliance (GCP, HIPAA, FDA), Data collection and integrity, Laboratory procedures, Study protocol execution, Adverse event reporting, SOP development, Project management, Mentorship
Preferred skills
Master's degree, 7+ years lab experience, Spanish fluency, Clinical Research Associate (CRA) certification
Technologies
Laboratory equipment, Electronic data capture systems, Regulatory databases
Responsibilities
Identify, screen, recruit, and enroll eligible research participants; Obtain informed consent and conduct study procedures; Coordinate regulatory activities including IRB submissions and biosafety documentation; Manage investigational medications and biological specimens; Collect, verify, and maintain research data; Mentor research coordinators and trainees; Develop instructional materials and SOPs; Manage multiple research projects and timelines.
Seniority
Senior, hands-on IC