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Clinical Research Associate
2 months ago
The Clinical Research Coordinator is a research professional who ensures oversight and compliance of both system-wide and local clinical research activities.
Works collaboratively with research personnel to ethically recruit and consent pediatric subjects and to appropriately collect and safeguard data.
The position's main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.
Key Responsibilities- Supports the investigator's development of SHC investigator-initiated research protocols.
- Supports the implementation of approved research protocols.
- Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice guidelines, applicable regulatory requirements, SHC policies and standards.
- Responsible for tracking all aspects of projects including all study, investigator, and IRB information, patient recruitment activity, and financial management.
- Coordinates the collection, statistical analysis, and dissemination of data results throughout a clinical study.
- Safeguards all participants involved in a research study supported and approved by the organization.
- Facilitates the local site's research programs and projects through collaborative, timely communication and teamwork.
- Required Education: Bachelor's degree in clinical research, science, or other healthcare field preferred.
- Required experience: At least one year of relevant research experience.
- Certification/licensure: CCRP or CCRC preferred.
- Additional experience: Working knowledge of the clinical research process and knowledge of ethical standards for research and a commitment to protect all participants.
