Clinical Research Assistant
California Retina Consultants
02.2022 - Current
- Educated patients regarding all facets of clinical study participation.
- Managed updates and input for patient information database.
- Assisted with research protocol development.
- Demonstrated advanced knowledge of federal regulatory compliance guidelines.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Followed informed consent processes and maintained records.
- Gathered, processed and shipped lab specimens.
- Performed duties in accordance with applicable standards, policies and regulatory guidelines to promote safe working environment.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Gained strong leadership skills by managing projects from start to finish.
- Learned and adapted quickly to new technology and software applications.
- Developed strong organizational and communication skills through coursework and volunteer activities.
