Clinical Research Coordinator I — Growth in Protocols

Baptist Health; Elizabethtown (KY); In loco; USD 42.000 - 66.000; Tempo pieno

Descrizione del lavoro

Baptist Health in Elizabethtown, KY is seeking a Clinical Research Coordinator I to support patient care under IRB-approved protocols. The role focuses on coordinating trial activities, maintaining documentation, and ensuring regulatory compliance in collaboration with investigators and hospital staff.

Qualified candidates will have 3+ years of clinical research or trial coordination experience, a health-related degree, and proficiency with EMR, Excel, Word, and PowerPoint.

Competenze

• Bachelor-level or technical diploma in biology, public health, pharmacy, or health-related field.
• Oncology experience not required but preferred.
• 3 years of experience in clinical research or as a clinical trial coordinator.
• Proficient with computers including navigating websites, electronic data systems, EMR, Excel, Word, PowerPoint.
• ACLS/BLS training required within 6 months.

Mansioni

• Coordinate patient care per IRB-approved protocol and regulatory requirements.
• Collaborate with investigators, research staff, and departmental stakeholders for trial coordination.
• Maintain clear documentation: track adverse events, concomitant meds, protocol deviations, and responses to study interventions.
• Work with senior staff to expand knowledge of research processes and organizational guidelines.

Conoscenze

Clinical research coordination

Team collaboration

Data documentation

Formazione

Biology/Public Health/Pharmacy/Health field

Strumenti

Excel

Word

PowerPoint

EMR systems

Descrizione del lavoro

Baptist Health in Elizabethtown, KY is seeking a Clinical Research Coordinator I to support patient care under IRB-approved protocols. The role focuses on coordinating trial activities, maintaining documentation, and ensuring regulatory compliance in collaboration with investigators and hospital staff.

Qualified candidates will have 3+ years of clinical research or trial coordination experience, a health-related degree, and proficiency with EMR, Excel, Word, and PowerPoint.