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Job Description:
Clinical Study Specialist IV
Contract Length: 12 months
Pay: $40/hr
Schedule: Part time - varied schedule
Location; Neenah, WI
Benefits: Medical, Vision, Dental
A Clinical Study Specialist is a professional who will coordinate and oversee clinical operations of research projects. This person will assess and evaluate subjects/subject safety. In compliance with established clinical research organizational policies/procedures, Good Clinical Practices plan, will conduct clinical research protocols. This person will work under the general supervision of the Principal Investigator/Clinical Research Manager (PI/CRM) responsible for the clinical studies.
Duties and Responsibilities:
- Obtain and review records for potential research subjects; maintain study records of research subjects that include documentation of study procedures and progress of research study subjects, following guidelines set forth by the protocol sponsors.
- Review recruited clinical study subjects for eligibility; schedule appointments and interviews and evaluate potential subjects.
- Instruct potential research subjects and responsible family members, nursing staff, and ancillary staff involved in research on the study procedures, treatments, and side effects.
- Educate subjects concerning protocol and explain informed consent procedures, including obtaining subjects written consent.
- Evaluate and assist in developing subject education materials and give subjects and/or family members instruction on test article administration and other study information.
Full-time, Part-time
$40.0/hr
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