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. Certified in GCP| ICH
Experienced in both medical practice and clinical research environments
Effective Communication with medical personnel, colleagues, and study participants
Experienced in multiple study areas, such as Device studies, Drug Studies
Verifications of all information pertaining to shipment receipt, use and return of device
Ensure compliance with internal policies and procedure
Time and task management, sound problem solving skills and flexibility
Detail-oriented Research Analyst with first-rate active listening
Committed to completing accurate and thorough competitive assessments
Ready to help team achieve company goals
Highly organized and thorough with good planning and problem-solving abilities
Ability to travel without Limitations
Strong Knowledge of Medical Terminology
Data collection processes