Clinical Research Coordinator I - Sarver Heart Center (COM-T)

Duties & Responsibilities

• Screen, recruit and enroll participants for assigned studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.
• Inform and instruct study participants concerning research protocol and complete the patient informed consent procedure.
• Assist with coordinating and performing research testing per protocol such as drawing blood, vital signs, EKGs, etc., includes processing and packaging of laboratory samples for shipment.
• Assess participants during research visit; perform initial review of study lab results; assess for any side effects or other problems; notify principal investigator of any participant reported side effects or problems.
• Complete case report forms for each study participant, and document medical data in the patient record and sponsor database. Ensure case report forms or other data collection/tracking tools are created if not provided by sponsor.
• Aid in preparing for and assisting with sponsor site visits and audits for assigned studies, including escorting visitors and providing requested documentation.
• Provide weekend and evening support for team coordination, communication, etc. to meet study protocol requirements.

Knowledge, Skills, And Abilities

• Demonstrated excellence in written and verbal communication.
• Ability to interpret and analyze data.
• Demonstrated ability to collaborate effectively with peers, patients, management, and internal and external stakeholders, fostering professional relationships that support operational efficiency, patient-centered service, and cross-functional project success.
• Knowledge of the principles, practices and techniques of clinical research skills.
• Proven ability to provide high quality, compliant research and ethical standards.

Minimum Qualifications

• Bachelor's degree or equivalent advanced learning attained through experience required.
• One (1) year of relevant work experience is required.

Preferred Qualifications

• Bilingual in English and Spanish.
• Experience in Human Subjects research.
• Experience with research protocols, development, and regulations.