Clinical Research Professional​/Clinical Research Professional II, UC Cancer Center

Clinical Research Professional / Clinical Research Professional II, UC Cancer Center

The University of Cincinnati Cancer Program is looking to fill a patient facing position as either a Clinical Research Professional or Clinical Research Professional II. This position will support the University's mission and commitment to excellence in our students, faculty, staff and all our activities. Please note this is a FULL-TIME, ON-SITE position, with incidental work from home opportunities.

Essential Functions:

• Under general supervision of the Clinical Research Manager, the Clinical Research Professional provides data management support and assistance to the University of Cincinnati Cancer Center Clinical Trials Office.
• Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.
• Follow established CTO workflows and CTO/UC Health standard operating procedures.
• Proactively review and locate source documentation for all study procedures.
• Accurately enters data from source documentation into electronic data capture (EDC) systems within 5 days of the patient visit.
• Proactively seeks to promptly resolve outstanding data queries and any issues through collaboration with clinical research coordinators (CRCs).
• Maintains and uses organizational systems to avoid delinquent data entry.
• Reviews all data entered into EDCs and subject charts to identify and help resolve any general quality issues.
• Conducts study participant follow-up as required per protocol.
• Communicates and collaborates within assigned research team and with principal investigators in a professional, helpful, and service-oriented manner.
• Acts as the primary point of contact for monitoring visits.
• Adheres to all UCCC CTO work instructions, SOPs, and study specific time frames.
• Able to independently maintain and meet form & database development milestones.
• Maintain/Update patients' status in the Clinical Trial Management System.
• Maintain Team's biospecimen collection kit inventory, re-ordering supplies as needed.

Minimum Requirements:

• Clinical Research Professional:
  Bachelor's Degree must be in a related field. Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement. One (1) year of related experience.
• Clinical Research Professional II:
  Bachelor's Degree must be in a related field. Seven (7) years of relevant work experience and/or other specialized training can be used in lieu of education requirement. Three (3) years of related experience.

Additional Qualifications Considered:

• Prior experience in clinical research coordination or clinical research data management, and Signal Path, Complion, Red Cap, Inform, Medidata RAVE, etc. systems is ideal.
• Highly comfortable with computer-based and online systems
• Must be able to interact and communicate with clinical research staff, PIs, and industry sponsors in a professional manner.
• High attention to detail and organizational ability and ability to prioritize tasks.
• Can accomplish work independently.
• Capable of advising and explaining information to others.
• Ability to manage moderately complex projects.
• Working knowledge of, and ability to apply, Good Documentation Practices, ALCOA, and ICH-GCP to data management and database design.
• Adherence to core values that were designed to create and maintain a positive work environment:
  Respect, Integrity, Teamwork and Excellence.

Physical Requirements/Work Environment:
Office environment/no specific unusual physical or environmental demands.

Compensation and Benefits:

UC offers an exceptional benefits package designed to support your well-being, financial security, and work-life balance. Highlights include:

• Comprehensive Tuition Remission
• Robust Retirement Plans
• Real Work-Life Balance
• Additional Benefits Include:

To learn more about why UC is a great place to work, please visit our Careers Page.