Knowledgeable Clinical Research Associate with several years of experience in documenting and assisting in clinical trials research. Clear, concise and effective written communication abilities. Thorough knowledge of FDA and GCP principles and regulations. Committed to providing support to the project team and executing responsibilities as instructed.
Original Clinical Research Associate with exceptional analytical and communication skills. Profound knowledge of FDA regulatory requirements. Superior organizational, record retention and time management skills. Talented at designing clinical research projects and project plans.
Successful at collecting specimens, overseeing medications and meeting with patients as part of clinical research trials. Proven abilities in managing schedules, results and records.
Flexible hard worker ready to learn and contribute to team success. Organized and motivated employee eager to apply time management and organizational skills in various environments. Seeking entry-level opportunities.