
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Documentation requirements
Research SOPs understanding
Specimen collections
Good Clinical Practices
Participant screening
Research experience
Study protocols
Electronic Data Capture
Adverse event reporting
Clinical trial management
Informed Consent Process
Time management abilities
Relationship Building
Decision-Making
Organizational Skills
Teamwork and Collaboration