Description:
Assist in the conduct and coordination of clinical trials by insuring compliance with clinical protocol requirements,
institutional and federal guidelines and department procedures under the direct supervision of the manager.
Responsibilities:
Job Requirement:
Assists with screening and consenting potential participants interested in research clinical studies.
Adheres to ongoing clinical trial protocol-specific procedures as well as good clinical practice and departmental standard
operating procedures.
Performs quality assurance checks on Informed Consent Forms, Case Report Forms and other research related
documents.
Assists Coordinators with maintaining monthly billing for study visits and documents appropriate fees on research referral
forms.
Assists Coordinators with the collection of data from patient charts, medical records, interviews, questionnaires and other
sources.
Tracks required patient visits and coordinators scheduling with front desk.
Completes, submits and organizes Case Report Forms.
Qualifications:Qualification
Experience Request:
2 years Experience in research regulatory experience strongly recommended preferred
Education:
High School Diploma required
Associates preferred
Additional Duties:
Additional duties as assigned may vary.
UFJPI is an Equal Opportunity Employer and Drugfree Workplace