Job Details

PS Clinical Research Coord Sr.

PS Clinical Research Coord Sr.
Job Summary
The Steele Center for Translational Medicine (SCTM) aims to identify therapeutic targets for age-related macular degeneration (AMD) and its newest initiative, glaucoma, two leading causes of visual impairment worldwide. The SCTM is comprised of an interdisciplinary team of basic and applied researchers, clinicians, clinical staff, and national/international collaborators. Our scientific efforts center around unique resources, including a collection of over 8,000 pairs of donated human eyes - complete with full genetic profiles, images, and ophthalmic and medical histories - and a large study cohort of AMD and glaucoma patients. This research aims to help better understand genotype-directed disease mechanisms, identify causal pathways and targets, and develop novel therapies to halt blinding eye diseases.'
Coordinates complex clinical trial activities and plays a critical role in the conduct of multiple research studies
Responsibilities
Essential Functions
- Evaluate processes to identify obstacles to successful recruitment and retention of study participants. Recommend and implement innovative approaches to maximize enrollment and optimize subject retention.
- Develop training and staff certification materials, procedures, and requirements. Assist the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study. Assist with training team members to include, but not limited to protocol requirements, schedule of visits, recruitment plan, execution of research plan, collecting adverse event information, maintaining study subject documentation. Maintain records and other documentation of training.
- Implement procedures to prevent future events, including staff education and retraining.
- Determine study visit and site/clinic work flows for studies/protocols.
- Develops QA/QC processes and conduct quality control activities (field/study visits, data queries)
- Helps to develop standard operating procedures.
- Assess and ensure participant safety and strict protocol implementation/adherence; oversee compliance with GCP guidelines, federal regulations, institutional policies and procedures, and internal SOPs.
- Assist in the selection and hiring process for study staff; mentor and train new or junior research staff; provide direction and oversee preparation of study staff.
The incumbent is expected to closely monitor use of experimental equipment and drugs. Because some subjects referred to participate on a research study have no other option for recovery, the incumbent must be aware of the subjects' condition, well informed in the use of study material (devices, equipment, etc.) and conscientious in his/her analysis of appropriate actions.
The incumbent is responsible for organizing coverage when not present to ensure protocol requirements are followed.
Comments Work Environment and Level of Frequency that may be required:
Nearly Continuously: Office environment.
Seldom: Infectious disease, oils (there is air or skin exposure to oils or other cutting fluids).
Physical Requirements and Level of Frequency that may be required
Nearly Continuously: Hearing, listening, talking.
Often: Repetitive hand motion (such as typing), walking, standing, sitting.
Seldom: Bending, reaching overhead.
The staff member must be able to demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served on his or her assigned unit. The individual must demonstrate knowledge of the principles of life span growth and development and the ability to assess data regarding the patient's status and provide care as described in the department's policies and procedures manual.
Minimum Qualifications
Bachelor's degree in a health science or related field or equivalency (one year of education can be substituted for two years of related work experience); plus, 4 years professional research experience and completion of University RATS Clinical Certification within one year of hire required. Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also required.
Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently is preferred.
Departments may require IRB CITI Course or IATA DGR training within a specified timeframe.
Departments may prefer a nursing degree for this position, which requires the incumbent to have two years related experience and possess a nationally recognized research compliance certification.
This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
Disclaimer This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
Preferences
Special Instructions
Requisition Number: PRN41681B
Full Time or Part Time? Full Time
Work Schedule Summary:
Department: 00870 - Ophthalmology-Research
Location: Campus
Pay Rate Range: $47,600.00 - $69,000.00
Close Date: 7/17/2025
Open Until Filled:
To apply, visit https://utah.peopleadmin.com/postings/181299
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