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Purpose: This person will be responsible for the conduct of multiple Oncology clinical research activities. Ideal candidate will have industry sponsored clinical trial experience. Must be knowledgeable on and have full understanding of good clinical practices (GCP) and regulations. Will be held accountable for adherence to all policies and procedures surrounding these processes and for maintaining up to date knowledge on these policies from IRB FDA ICH GCP or other sources
*FL RN License Required
*On-Site
*Oncology Experience
What you will do:
Assist in the recruitment of study participants.
Screen patient charts to identify eligible study patients.
Review all prospective protocol patients charts to evaluate protocol eligibility advise investigators of needed tests to complete pre-treatment work-up.
Assist in coordinating the collection of all protocol required laboratory testing (i.e. blood bone marrow urine etc.) Extract data from study participants source documents.
Assist the investigators in evaluating documenting and reporting adverse events and other safety related data.
Conduct telephone screening calls for patients inquiring about their participation in clinical trials. Interact and educate patients and families to help them gain an understanding and alleviate any
apprehension regarding the studies.
Obtain written informed consent from patient allowing for free expression of fears questions etc. to ensure patient understanding.
Ensure the accuracy and completeness of site regulatory documentation including but not limited to IRB and FDA approvals and reports and adverse event documentation.
Participate in site initiation monitoring and close out visits.
Minimum Qualifications:
Education:
Licensure/Certification:
Position Highlights and Benefits
Ministry/Facility Information:
Legal Info:
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race color sex age national origin religion sexual orientation gender identity status as a veteran and basis of disability or any other federal state or local protected class.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Full-time
Full-time