Research Associate - Urology

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.
• 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

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