Research Associate-Radiology-Full-Time-Days

Responsibilities

• 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.
• Affords support to Coordinators with maintaining monthly billing for study visits and documenting appropriate fees on research referral forms.
• Affords support to 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

• Experience in research regulatory experience strongly recommended preferred.
• High School Diploma required.
• Associates degree preferred.

Additional Duties

Additional duties as assigned may vary.