
Versatile, detail-oriented clinical research and medical professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for clinical trials. Multitasks and prioritizes workload both independently and in collaboration. Highly organized and thorough with good planning and problem-solving abilities. Bilingual in English and Spanish.
Thorough knowledge of medical conditions and medications
Technical Writing
Patient Assessments
Monitoring patient progress
Regulatory compliance
Study protocols
Trial management
Electronic Data Capture