Experience

Teal Health

• United States
• Hospitals and Health Care
• 1 - 100 Employee

• Clinical Trial Manager

  • Apr 2023 - Present



CRISPR Therapeutics

• United States
• Biotechnology Research
• 300 - 400 Employee

• Senior Clinical Trial Associate

  • Jan 2022 - Apr 2023

• Clinical Trial Associate

  • Jan 2020 - Jan 2022

• Clinical Trial Coordinator

  • Feb 2019 - Jan 2020



Clayton Eye Center

• United States
• Medical Practices
• 1 - 100 Employee

• Clinical Research Coordinator II

  • Jul 2016 - Feb 2019

  Provide assistance in daily clinical trials activities, such as performing administrative responsibilities, researching and collecting data (source documents), and preparing case reports. Recruit specialists and update information into system as necessary. Maintain interactions with Institutional Review Board (IRB). Evaluate and review patients’ medical histories and charts as well as collect, process, and send human biological samples to laboratories. -Enable clinical studies by coordinating efforts and aiding physicians, medical staff, and patients with procedures and study visits while complying with protocols and safety measures.-Carry out numerous medical procedures and tests, including visual acuity, visual field, optical coherence tomography (OCT), and blood draws.-Manage and keep up detailed study logs and progress reports, analyzing and tracking clinical trials and regulatory submissions. -Instruct and guide less-experience coordinators on specific processes, clinical studies, and researches.-Work directly with monitors during site initiation, interim, and study close-out visits. Show less

• Clinical Research Coordinator I

  • Sep 2015 - Jul 2016

  Aided Principal Investigator by coordinating and supporting research studies and trials for ophthalmic medications and devices; ensured compliance with established protocols, federal regulations, and institutional policies. Documented safety issues during clinical studies.-Collaborated in participants’ screening and enrolling processes, gathering key data for researches, distributing experimental treatments, and reviewing databases. -Evaluated patients’ medical histories and performed visual acuity and visual field tests; handled biological substances in a proper and secure manner. -Monitored and managed study records, case reports, regulatory forms, medication administration, and other sensitive information, assuring accuracy and patients’ well-being and security. Show less