Posted
Thurs., Aug. 29
Organization
Fromer Eye Centers
Position Description
Clinical Research Assistant needed for conducting scientific studies in Optometry/Ophthalmology field. The Research Assistant will identify subjects in clinical trials and collect data, evaluate results, monitor clinical trials, and take notes on activities.
The Research Assistant will audit trials and ensure clinical trial protocols are in compliance. They transfer data from paper formats to electronic formats in organized spreadsheets with large numbers, if needed. They also will be responsible for curating data directly from research.
The Clinical Research Assistant will also draft informed consent forms for trials and prepare correspondence, documentation, or presentation materials on research findings. They prepare interview questions, summarize results, perform literature reviews, respond to emails related to the research, attend project meetings, and prepare progress reports.
The Clinical Research Assistant will also monitor a project budget and check its progress.
Responsibilities include:
- Gather, analyze and interpret data to identify opportunities to improve clinical research.
- Participate in the development of protocols and case report forms as assigned.
- Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned.
- Independently perform CRF review, query generation and resolution against established data review guidelines on client data management systems as assigned by management.
- Lead and participate in conferences related to the project and/or its progress. Present research findings in the meetings, conferences, and professional societies.
- Provide data analytic support for audits and monitor visits.
- Using established procedures and working under immediate supervision, perform assigned data analytic related tasks.
- Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
- Perform literature reviews and create bibliographies for reports and papers.
Position Requirements
The candidate will need a bachelor's degree in business administration, science, health science, psychology, or related field; certification by the state as licensed through the American Society for Clinical Laboratory Science; Strong command of the English language; Proficient with Microsoft Suite; Advanced understanding of HIPAA regulations; Excellent decision-making abilities and ability to embrace a fast paced and dynamic environment daily.
Time Commitment
6 months
Compensation
$17-$20/hr
Apply
Email [email protected] with resume and cover letter.
