Clinical Research Coordinator: Driving Impactful Trials

St. Elizabeth; Edgewood (KY); Sur place; USD 55 000 - 75 000; Plein temps

Résumé du poste

St. Elizabeth in Edgewood, KY seeks a Clinical Research Coordinator to coordinate studies under the principal investigator, open new studies, educate staff and participants, and ensure regulatory compliance.

The role involves screening and enrolling subjects, obtaining informed consent, data collection, and documenting in medical records while maintaining privacy and protocol adherence.

Qualifications

• Proficiency with Excel, Word, Outlook and PowerPoint.
• Ability to manage multiple tasks and meet deadlines.
• Strong collaboration with physicians and regulatory staff.

Responsabilités

• Coordinate clinical research studies with principal investigators.
• Screen and enroll subjects; obtain informed consent.
• Ensure regulatory compliance and data submission per protocol.

Connaissances

Excel

Word

Outlook

PowerPoint

Formation

Associate degree in related field

Description du poste

St. Elizabeth in Edgewood, KY seeks a Clinical Research Coordinator to coordinate studies under the principal investigator, open new studies, educate staff and participants, and ensure regulatory compliance.

The role involves screening and enrolling subjects, obtaining informed consent, data collection, and documenting in medical records while maintaining privacy and protocol adherence.