Human Subject Research Coordinator Trainee
Rochester, New York
Employer: University of Rochester
Industry: Healthcare Professional
Salary: $18.65 - $26.11 per hour
Job type: Full-Time
Opening
Full Time 40 hours Range URG 104 Clin & Trans Science Institute
Schedule
8 AM-4:30 PM
Responsibilities
GENERAL PURPOSE:
Assists with the activities associated with human subject research.
RESPONSIBILITIES:
QUALIFICATIONS:
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled
Pay Range
Pay Range: $18.65 - $26.11 Hourly
The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
Full Time 40 hours Range URG 104 Clin & Trans Science Institute
Schedule
8 AM-4:30 PM
Responsibilities
GENERAL PURPOSE:
Assists with the activities associated with human subject research.
RESPONSIBILITIES:
- Assists with the administrative details required to initiate and conduct human subject research, including receiving, distributing and explaining study information, such as protocol and human subject recruitment materials, to immediate team members and relevant others.
- Tracks regulatory and other documents, such as consent forms and CRFs, and ensures these are complete, accurate and available for review.
- Learns and applies the details of the protocol, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion and adverse event reporting.
- Assists in human subject recruitment and screening activities, including reviewing study site patient databases and office records for patients that meet the protocol inclusion criteria, processing biospecimens and conducting telephone interviews to screen potential study candidates.
- Tracks research participant adherence with protocol requirements, such as taking of medications, proper use of device and/or other interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board (IRB), Sponsor and/or any other required recipients or entities.
- Tracks and documents the dispensing and returning of study materials, such as study drugs and devices.
- Keeps current with industry standards, best practices and trends in therapeutic areas relevant to research studies.
QUALIFICATIONS:
- Associate's degree required
- No previous experience required
- or equivalent combination of education and experience required
- Experience as a Phlebotomist preferred
- Word processing and data analysis software preferred
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled
Pay Range
Pay Range: $18.65 - $26.11 Hourly
The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
Created: 2024-09-01
Reference: 255013
Country: United States
State: New York
City: Rochester
ZIP: 14608
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