

Versatile clinical research professional knowledgeable about coordinating regulatory submissions, regulatory affairs expertise, day to day clinical trial operations including patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in clinical research operations with excellent quality .
Interpersonal Communication
Organisation and Time Management
Teamwork and Collaboration
Regulatory affairs
Regulatory Submission
Clinical Research
Medical writing
Document managememt
Trial operations
Strategic initiatives