Cottage Health is seeking a Clinical Research Coordinator I- Non-RN . The Clinical Research Coordinator I- Non-RN is responsible for all study management tasks for studies in which they are assigned to as the Primary Coordinator. Accountabilities include:

• Acting as a liaison between the Principal Investigator (PI), Institutional Review Board (IRB), other hospital departments, and study participants for study management.
• Provides study information to physicians, nurses, pharmacists, and lab personnel.
• Arranges in-service trainings as appropriate.
• Responsible for implementation, data management, and follow up of clinical trials to ensure data accuracy, study participant safety, confidentiality, protocol compliance, and regulatory compliance as required by the clinical trial protocol and the study sponsor.

QUALIFICATIONS

All job qualifications listed indicate the minimum level necessary to perform this job proficiently.

LEVEL OF EDUCATION

Minimum: Bachelor’s Degree in biomedical or healthcare related field or Bachelor’s Degree in unrelated field with relevant research experience.

TECHNICAL REQUIREMENTS

Minimum: Excellent communication and writing skills. Basic Microsoft Word, Excel, PowerPoint, and Outlook skills.
Preferred: Familiarity with HIPAA regulations and regulations governing human subjects in research. Demonstrated knowledge and understanding of the IRB process. Working knowledge of scientific and medical concepts and terminology, and strong familiarity with biomedical research protocols.

YEARS OF RELATED WORK EXPERIENCE

Minimum: One (1) year of experience in research/healthcare environment (i.e. academic research experience).
Preferred: Two or more years of research experience

• Acting as a liaison between the Principal Investigator (PI), Institutional Review Board (IRB), other hospital departments, and study participants for study management.
• Provides study information to physicians, nurses, pharmacists, and lab personnel.
• Arranges in-service trainings as appropriate.
• Responsible for implementation, data management, and follow up of clinical trials to ensure data accuracy, study participant safety, confidentiality, protocol compliance, and regulatory compliance as required by the clinical trial protocol and the study sponsor