Laboratory Research Assistant
About The Position
The Laboratory Research Assistant (LRA) will join our dedicated clinical laboratory team and be responsible for the analysis and data collection for clinical laboratory device trials. They will collect data for clinical device trials and specimen procurements, while preparing and maintaining regulatory forms and records, supply accountability, case report forms (CRFs), shipping records, de-identification and ID crosswalk. They will participate in site sponsor visits, trainings, and inspections. They will have input into the development of workflow procedures. They will maintain the quality and integrity of the clinical data through completion of eCRF database and on-site source verification records while working with sponsors to resolve queries and helps ensure all study deliverables are completed per study timelines. The LRA will record and maintain trial data files for studies being cognizant of protocol requirements, source documentation, EDC system, case report form completion, and workflow. They will understand the patient consent practices and follow good clinical practice guidelines. Work Locations: UHS Wilson Medical Center, Johnson City, NY Vestal 3 Administrative Building, Vestal, NY There is more than one location associated with this position. This is either because there are multiple openings at different sites, or the successful candidate will be required to float across multiple UHS facilities. Your recruiter and hiring manager will clarify expectations during the interview process. Work Shift and Schedule: This is a per diem position, which means you will work on an as needed, agreed upon basis. Working hours will be assigned by your manager. Compensation Range: $17.05 - $22.17 per hour, depending on experience This position is not eligible for benefits.
Requirements
- High school diploma and at least 1 year of experience working in health care
Nice To Haves
- Associates degree in scientific discipline or health care field
- Direct experience working with patients in a healthcare setting
- Knowledge of basic medical terminology and clinical skills
- Proficient with Microsoft Office, general computer systems, and ability to learn other applications as needed
- Excellent written and verbal communication skills
- Good customer service skills
- High level of organization, ability to multitask, ability to work as a team and independently
Responsibilities
- Analysis and data collection for clinical laboratory device trials
- Collect data for clinical device trials and specimen procurements
- Preparing and maintaining regulatory forms and records, supply accountability, case report forms (CRFs), shipping records, de-identification and ID crosswalk
- Participate in site sponsor visits, trainings, and inspections
- Input into the development of workflow procedures
- Maintain the quality and integrity of the clinical data through completion of eCRF database and on-site source verification records while working with sponsors to resolve queries and helps ensure all study deliverables are completed per study timelines
- Record and maintain trial data files for studies being cognizant of protocol requirements, source documentation, EDC system, case report form completion, and workflow
- Understand the patient consent practices and follow good clinical practice guidelines
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What This Job Offers
Career Level
Entry Level
Education Level
High school or GED
