Certified Clinical Research Coordinator (CCRC) is a professional certification given to individuals who have met the eligibility criteria and passed the certification exam offered by the Association of Clinical Research Professionals (ACRP). CCRCs are responsible for the coordination and management of clinical trials in compliance with regulatory requirements and protocol specifications. CCRCs are trained in Good Clinical Practice, study design and ethics, subject recruitment and retention, data management, and safety monitoring, among other skills. The CCRC certification demonstrates a standard of knowledge and competence in clinical research coordination.

Clinical Research Coordination refers to the planning, organization, and oversight of activities that support clinical studies. It includes managing study procedures, maintaining records, coordinating with research teams and participants, and helping ensure that work follows approved protocols and applicable requirements. This skill is used in work settings to keep research activities organized, accurate, and aligned with study timelines and data collection needs.

Human subject research refers to scientific investigations that involve individuals as participants, and their experiences, behaviors, or biological specimens as study objects. Conducting research on human subjects requires specialized knowledge and skills to ensure ethically and legally sound practices, and to protect the rights, welfare, and privacy of participants. This includes obtaining informed consent, conducting risk assessment, addressing confidentiality and data security, and complying with regulatory and ethical guidelines. Human subject research is critical for advancing knowledge in many fields and requires careful and responsible conduct to maintain trust and integrity.

Institutional Review Board (IRB) is a committee that is responsible for reviewing and approving research involving human subjects. IRB members are typically experts in research ethics and have the authority to approve, modify, or disapprove research protocols to ensure that they comply with ethical standards and government regulations. The IRB's goal is to protect the welfare and rights of human research participants and ensure that any risks associated with the research are minimized. As such, being a member of an IRB requires specialized skills and knowledge in research ethics, human subjects protection, and regulatory compliance.

Research Support involves providing resources, tools, and assistance to facilitate the planning, execution, and analysis of research activities. It is used to enhance data collection, improve study design, and ensure the validity of research findings.