Duties/Responsibilities:
- Participates in the training required to follow the protocols of research studies.
- Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators of problems, or assists in problem resolution efforts such as protocol revisions.
- Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
- Participate in the case report forms as assigned.
- Assist in documentation for audits and monitor visits.
- Using established procedures and working under immediate supervision, perform assigned data analytic related tasks.
- Communicate with research subjects regarding the research activities they are participating in to help scheduling of activities.
- Address queries that are flagged by the data management system.
Required Skills/Abilities:
- Knowledge of biological and medical terminology.
- Understanding of the principles of administration and management.
- Phlebotomy certification is preferred.
Education and Experience:
- High School Diploma or GED.
- Clinical research experience preferred.
Job Type: Full-time
Pay: $17.00 - $20.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
- Night shift
- Overnight shift
Application Question(s):
- What is your salary requirement per hour?
Education:
- High school or equivalent (Preferred)
Experience:
- Clinical research: 1 year (Preferred)
- Phlebotomy: 1 year (Preferred)
Language:
- Spanish (Preferred)
License/Certification:
- Driver's License (Required)
Shift availability:
- Overnight Shift (Required)
- Night Shift (Required)
Work Location: In person