Clinical Data Coordinator- Cardiology

Clinical Data Coordinator- Cardiology

Department: SOM KC Division of Cardiovascular Diseases CCR

Position Title: Clinical Data Coordinator- Cardiology

Job Family Group: Professional Staff

Job Description Summary: The Clinical Data Coordinator (CDC) will collect, abstract, review, document and monitor data related to clinical research studies. Collect, abstract, review, document, and monitor data related to clinical research projects. Additional responsibilities include involvement in the coordination of study start-up requirements and other duties that may be assigned by management staff.

Job Responsibilities

• Responsible for overall knowledge of protocols as assigned.
• Create and maintain logs, data base or data registry.
• Work collaboratively with the physician, nurse clinicians, pharmacy, and laboratory personnel to ensure data is obtained per protocol and correct.
• Communicate regarding patient data, status and protocol requirements with research staff.
• Conduct clinical trial in accordance with ICH/CFR/GCP and responsible for all data completion; query resolution for assigned protocols.
• Assist with the identification and reporting of Adverse and Serious Adverse events in accordance with ICH/CFR/GCP and specific protocol.
• Attend study specific training required by position, to include but not limited to Study Initiation.
• Prepare and provide patient status report.
• Research and resolve data discrepancies; coordinate any database activities and participate in customer audits and process improvement initiatives.

Required Qualifications

Work Experience: Four years of experience with clinical data entry, medical/clinical research and medical terminology. Relevant education may be substituted on a year-for-year basis.

Preferred Qualifications

Education: Bachelor's degree in applicable field of study.

Certifications: Research certification such as: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or Association of Clinical Research Professionals (ACRP).

Work Experience:

• Experience in department field of research, reviewing patient data/medical records or working with research participants.
• Experience with database software, SPSS statistical software and REDCap.

Skills

• Computer skills.
• Communication.
• Interpersonal skills.
• Organization skills.
• Attention to detail.
• Multi-tasking.

Required Documents

• Resume
• Cover Letter