Clinical Research Coordinator IV - R104647
at University of Louisville
Louisville, KY 40208, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Sep, 2024 | USD 31 Hourly | 10 Jun, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
MINIMUM REQUIREMENTS:
Bachelor’s degree in a related filed or an equivalent combination of education and experience.
POSITION DESCRIPTION:
Become part of the Clinical Trials Unit (CTU) Clinical Team supporting GI and Hepatology research as a Clinical Research Coordinator IV.
Duties and Responsibilities:
- Coordinate the implementation of clinical research projects; organize the clinical research team; and serve as an advocate for study subjects.
- Develop a recruitment plan for each assigned protocol with the research team.
- Identify potential sources for subjects and establish appropriate networks to support referrals.
- Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility.
- Educate subjects on protocol-related procedures/assessments in which they must participate as a study subjects.
- Collect, organize, and maintain data and test results for source documentation of all research subjects.
Responsibilities:
- Coordinate the implementation of clinical research projects; organize the clinical research team; and serve as an advocate for study subjects.
- Develop a recruitment plan for each assigned protocol with the research team.
- Identify potential sources for subjects and establish appropriate networks to support referrals.
- Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility.
- Educate subjects on protocol-related procedures/assessments in which they must participate as a study subjects.
- Collect, organize, and maintain data and test results for source documentation of all research subjects
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
A related filed or an equivalent combination of education and experience
Proficient
1
Louisville, KY 40208, USA