Clinical Research Coordinator - Non-RN Trials

University of Utah; Salt Lake City (UT); Presencial; USD 30.000 - 83.000; Jornada completa

Descripción de la vacante

The University of Utah invites applications for a Clinical Research Coordinator (Non-R.N.) in Salt Lake City. This full-time, on-site role supports the Surgical Research department, coordinating study implementation, regulatory compliance, subject enrollment, and data management to help investigators meet study objectives.

The position involves budget oversight, regulatory submissions, participant coordination, and staff supervision, with a diverse set of responsibilities across IRB, FDA, NIH

Formación

• Equivalency Statement: 1 year of higher education can be substituted for 1 year of directly related work experience.

Responsabilidades

• Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
• Develops study budgets; monitors budget expenses and billing for allied services; negotiates payment schedule with sponsor and fees for internal services.
• Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance. Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.
• Recognizes, tracks and reports adverse events and protocol deviations.
• Prepares for and coordinates site visits made by sponsors or federal agencies during course and at the close of the study.
• Represents the research program at meetings, national and international research consortia.
• Prepares, submits and maintains IRB , FDA , NCI , NIH , NSF and/or other regulatory documents and research correspondence.
• Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues.
• Supervises, mentors and trains new or junior research staff.
• Coordinates with referring physicians to provide information regarding available research projects and to maintain a strong referral basis.
• Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
• Assists the Principal Investigator in the development of study protocols.

Educación

Equivalency Statement

Bachelor's degree or higher

Descripción del empleo

The University of Utah invites applications for a Clinical Research Coordinator (Non-R.N.) in Salt Lake City. This full-time, on-site role supports the Surgical Research department, coordinating study implementation, regulatory compliance, subject enrollment, and data management to help investigators meet study objectives.

The position involves budget oversight, regulatory submissions, participant coordination, and staff supervision, with a diverse set of responsibilities across IRB, FDA, NIH