Job Duties -Participates in patient recruitment ensuring proper informed consent, eligibility requirements are met and enrolls patient onto trial.
Manage patients on research study ensuring all study required visits are completed per protocol.
Maintains compliance with protocol requirements and all applicable regulatory requirements.
Performs accurate and complete data entry, case report form completion and query management.
Ensure data is entered into clinical trial monitoring systems.
Participate in monitoring visits, site initiation visits and close-out visits as needed.
Attends required training, maintains applicable certification and/or licensure as required.
Attends regularly scheduled team meetings. Performs other duties as assigned -Ensures regulatory compliance of clinical research program.
Develops system for data collection and management of clinical research program registry information.
Duties performed include directly interacting with or caring for patients, Directly interacting with or caring for human-subjects research participants,
Research experience preferred.
Benefit Conditions:
Contract Renewal:
COVID-19 Precaution(s):
- Personal protective equipment provided or required
- Sanitizing, disinfecting, or cleaning procedures in place
Work Remotely
Job Type: Full-time
Pay: $38,400.00 - $40,000.00 per year
Benefits:
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Work Location: In person
