Clinical Research Professional I

About the role

The Clinical Research Professional I coordinates selected specific aspects of clinical research studies. This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study. Preferred but Not Required: Bilingual (Spanish/English) Additional Information: The Clinical Research Professional I coordinates selected specific aspects of clinical research studies. This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study. Required Education: High school diploma or GED or equivalent Recommended Education: Bachelor's degree in a related field of study. Required Work Experience: High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED. Recommended Work Experience: Required Certifications: Recommended Certifications: Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates 1. Recruits and screens patients for enrollment eligibility and participation in research projects. Obtains consent for participation in accordance with all government regulations and internal policies/procedures. 2. Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms. Creates databases and performs date entry into the database. 3. Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information. 4. Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research. 5. Facilitates and improves collaboration with other departments to facilitate research across the continuum. 6. Coordinates/collects requested data for sponsor review during site visits. Assists study monitor(s) in chart and case report form review. 7. Maintains files and study documentation according to institutional and regulatory standards 8. Performs other duties as assigned.