GENERAL SUMMARY
The Contingent Clinical Research Coordinator I (CRC I) position in the Emergency Center Research is responsible for coordinating appropriate research studies, including participant recruitment, data collection/management and follow up.
ESSENTIAL DUTIES
1. Participates in research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable.
2. Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents.
3. Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods.
4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
5. Practice BH hospitality standards. Maintain professional and technical knowledge.
6. Research participant/family communication, protect patient confidentiality.
STANDARD REQUIREMENTS
A. Education / Training: Bachelor's degree in health-related field with two to five years relevant clinical experience OR two to five years research experience with National Research Certification (SoCRA or ACRP). If applicable, department-specific certification and/or experience may also be required.
B. Work Experience: 2-5 years relevant clinical research experience.
C. Certification, Licensure, and Registration: National Certification (SoCRA or ACRP) required, within 2-5 years, if not met in Education/Training above. Basic Life Support (BLS) Certification required.
D. Other Qualifications: Expert database and computer skills: Microsoft Office (Word, Excel), Outlook, HDS, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.
ACKNOWLEDGEMENT OF EMPLOYMENT UNDER RESEARCH GRANT