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Description:
Must haves:Recruit, Screen, Enroll subjects in to clinical trails Explain Informed Consent process Document adverse events Collect study documents, protocols, regulatory documents, informed consents, case report forms and source documents Prepare the Institutional Review Board, IRB applications
Skills:
enrollment, Informed Consent, patient, oncology, patient consenting, clinical research coordinator, clinical trial, gcp, edc, Chart review, Emr, Patient recruitment, Clinical research, oncology, Pre-screening patients, Medical record, Data entry, Regulatory
Top Skills Details:
enrollment, Informed Consent, patient, oncology, patient consenting, clinical research coordinator, clinical trial,gcp,edc,Chart review,Emr,Patient recruitment
Additional Skills & Qualifications:
BA/BS preferred - Experience with in-hospital clinical research -2 years clinical research experience required - Experience with adverse event reporting -Experience with patient recruitment and consenting -Effective communication and writing skills -Knowledge of IRB and human research protection regulations
Experience Level:
Intermediate Level
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Other
$69k-89k (estimate)
12/21/2022
04/27/2024
The following is the career advancement route for Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator. You can explore the career advancement for a Clinical Research Coordinator below and select your interested title to get hiring information.