Reviews specimen documentation and regulatory requirements
Verifies and inputs specimen data
Develops, onboards, coordinates, and manages clinical trial study and research objectives, meeting requirements and following regulatory guidelines
Job Summary
Develops, onboards, coordinates, and manages clinical trial study and research objectives, meeting requirements and following regulatory guidelines.
Reviews specimen documentation, verifies and inputs data, organizes studies, and monitors specimen-related data for accuracy and discrepancies.
Serves as a point of contact, interacts with internal and external teams, and provides feedback to resolve issues and complete activities per trial requirements.
Matching Summary
Develops, onboards, coordinates, and manages clinical trial study and research objectives, meeting requirements and following regulatory guidelines.
Skills & Requirements
Must-have
Develops and manages clinical trial studies
Reviews specimen documentation and regulatory requirements
Verifies and inputs specimen data
Organizes clinical research studies and monitors data
Manages projects and ensures accurate documentation
Creates and modifies reference documents for data collection
Serves as a point of contact and project coordinator
Nice-to-have
Solution-driven mentality
Promotes cohesive, positive, and team-oriented work environment
Adapts to various cultural and work-style differences
Helps others stay productive, motivated, and creative
Key Requirements
Bachelor’s Degree in Science, Business Administration, or related field
Three years of academic or professional experience in clinical research or healthcare field
Three years of experience in clinical trials, oncology, or healthcare business development
Working knowledge of PCs and word processing and data management software