1. Compares protocols and sponsored projects to confirm consistency between funding proposals/awards and approved protocols. 2. Documents established congruency between funding proposals and approved protocols. 3. Facilitates and/or assists with resolution of any inconsistencies between funding proposals and approved protocols. 4. Serves as a liaison between the Grants and Contracts offices, investigators, and business managers to resolve congruency issues in a timely manner. 5. Attends meetings and presents issues when necessary that were identified during congruency review. 6. Serves as a resource and provides technical assistance to investigators and their staff. 7. Provides analytical and technical support related to establishing and recording protocol/grant congruency, as needed. 8. Monitors federal and state regulations for new guidance, updates, or policies. Maintains a high degree of knowledge on these requirements to determine actions and follow directives that may be required to ensure University compliance with congruency review and reporting requirements. 9. Develops, implements, and manages internal practices that ensure compliance with federal requirements. 10. May perform other duties as assigned.

Required Skill/ability 1:  Proven work experience in a research or clinical setting.

Required Skill/ability 2:  Ability to work in a complex research and clinical setting on multiple projects in different stages of development; Excellent attention to detail. Ability to set priorities.

Required Skill/ability 3:  Proven strong interpersonal skills. Ability to communicate effectively and collaborate with all levels of clinical team members, patients, providers, and external funders. Strong written and oral communication skills.

Required Skill/ability 4:  Flexibility and willingness to learn new skills/ adapt to different settings (outpatient, inpatient, study specific requirements).

Required Skill/ability 5:  Proficiency with MS Office suite.

Preferred Education:  Knowledge of clinical research regulatory requirements, familiarity with electronic medical record system, database navigation. Prior clinical trial experience.

Work Week:  Standard (M-F equal number of hours per day)

Posting Position Title:  Coordinator 4, Research Support

University Job Title:  Clinical Research Coordinator

Preferred Education, Experience and Skills:  Knowledge of clinical research regulatory requirements, familiarity with electronic medical record system, database navigation. Prior clinical trial experience.

Bachelor's degree in a relevant academic/scientific field and a minimum of 3 years of related research support experience; or the equivalent combination of education or experience.

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