T221591 - University of Alabama at Birmingham

The University of Alabama at Birmingham (UAB), Urology Chair Office, is seeking a Clinical Research Coordinator III. The Clinical Research Coordinator III will perform clinical research in female pelvic and reconstructive surgery (FPMRS), general urology, kidney stones/endourology, oncology, and reconstructive urology.

General Responsibilities

• To serve as a lead coordinator by providing oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.
• To coordinate and manage the research study lifecycle from start-up through close-out.
• To coordinate and conduct all applicable clinical and administrative activities required by the protocol such as screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under the auspices of Good Clinical Practice (GCP).

Key Duties & Responsibilities

1. Manages all aspects of the research program and clinical studies including education/training.
2. Develops protocol-specific systems and documents including process flows, training manuals, SOPs, and CRFs.
3. Prepares study budgets as needed.
4. Coordinates studies of all complexities.
5. Acts as a consultant within the area of clinical expertise.
6. Provides a lead role in determining participant eligibility.
7. In addition to creating study documentation, may provide oversight to junior staff members as well as for items such as source, lab, and pharmacy orders, flowsheets, and adverse events.
8. In conjunction with the PI or Director, interprets and applies current research findings in the area of clinical specialty and reports findings in professional journals and local, state, and national conferences.
9. Identifies various stakeholders to ensure adequate design, implementation, and testing of study aims.
10. Prepares and submits multiple levels of research documentation (i.e. IRB, IND, or FDA submissions, educational materials, reports, grant renewal reports, and study forms).
11. Collects information to determine study feasibility.
12. Makes recommendations to investigators and oversight organizations, as appropriate.
13. Maintains compliance with federal, state and accrediting agencies (sponsors), including maintaining any required documentation.
14. May conduct literature reviews and contribute to assessing solutions for operational shortcomings of data procurement in protocol design.
15. Prepares for and leads team meetings.
16. Disseminates information related to studies, training, and general research operations as needed.
17. Assists colleagues in identifying efficiencies and improving processes.
18. Arranges multidisciplinary evaluations.
19. Performs other duties as assigned.

Annual Salary Range:%2460,835 - %2479,000

Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

Preferences

• Clinical research in Urology is strongly preferred.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, religion, sexual orientation, gender identity, gender expression, and veteranrsquo;s status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UABrsquo;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.