Clinical Research Coordinator Cardiology

About the role

The Department of Medicine, Division of Cardiology, seeks a Clinical Research Coordinator to support and coordinate clinical studies. Responsibilities include assisting with the operationalization of investigator-initiated studies, managing industry-sponsored research, and contributing to a cardiology cohort study.

Responsibilities

• Support and coordinate clinical studies under the supervision of the Clinical Research Supervisor or Manager
• Prepare and submit protocols through the CHR online iMEDris system
• Build and maintain strong working relationships with sponsors, monitors, principal investigators, and other key stakeholders
• Manage patient recruitment and consent processes
• Ensure compliance with ICH/GCP and FDA requirements for INDs, IDEs, and NDAs
• Handle confidential information appropriately and maintain positive interpersonal skills
• Collaborate with medical staff and other departments to ensure project success
• Travel for investigator meetings (limited)

Requirements

• High school graduate with relevant experience and skills
• Attention to detail and strong interpersonal skills
• Excellent verbal and written communication skills
• Ability to work independently and prioritize multiple projects
• Positive interpersonal skills and problem-solving abilities
• Willingness to travel (limited)

Qualifications

• Demonstrated ability to handle confidential information appropriately
• Experience in clinical cardiology and clinical/cardiovascular research
• Applied knowledge in drug and/or device trials
• Understanding of patient population and realistic expectations for participation
• In-depth knowledge of ICH/GCP and FDA requirements
• Experience with electronic medical records, EPIC preferred
• Knowledge of biospecimen collection, processing, and transport
• Experience with database building/analysis and data management using Access, Stata, SASS/SPSS, and Teleform programming platforms
• Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals
• Experience applying Good Clinical Practice Guidelines, HIPAA, and CHR regulations
• Effective cash handling procedures and environmental health and safety training

Skills

• Strong organizational and time management skills
• Ability to work in a fast-paced environment
• Effective communication skills
• Confidentiality and HIPAA compliance
• Interpersonal and problem-solving skills

Benefits

Not specified

Pay

Not specified

Schedule

Not specified