Assistant Clinical Research Coordinator
Responsibilities
Assist in coordination and execution of clinical research protocols; recruit, screen, and enroll study participants; coordinate and schedule study visits; collect and maintain clinical research data; communicate with study participants; monitor study progress and report adverse events; support preparation and submission of regulatory documents; draw, process, and ship laboratory specimens; scan, upload, file, and maintain study records.
Required skills
High school diploma or equivalent; basic knowledge of clinical research principles, medical terminology, and healthcare environments; strong organizational, time management, and attention-to-detail skills; ability to communicate clearly and professionally; ability to work collaboratively in a fast-paced environment.
Preferred skills
Associate's degree or higher in a health-related field; experience in clinical research or healthcare settings; knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines; experience with participant recruitment, screening, and informed consent; proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office; Certified Medical Assistant (MA) or Phlebotomist; Current CPR/BLS certification; Certification as a Clinical Research Coordinator (CCRC) or willingness to obtain it.
Technologies
Electronic data capture systems; clinical trial management software; Microsoft Office (Excel, Word, PowerPoint).
Seniority
Entry-level to Mid-level (Assistant role).
Domain
Clinical Research / Healthcare.