Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring six years of related experience to a challenging new role. Knowledgeable Clinical Trial Associate adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
Clinical drug trials
Clinical trial expertise
Clinical inventory control
Clinical documentation management
Clinical study reporting
Informed consent
Good Clinical Practices
Research SOPs understanding
MS Office
Data Entry
Study protocols
Interpersonal Communication
SA & ICH (R2) Good Clinical Practice for Clinical Trial Sites Course