Clinical Research Coordinator
Join an organization that operates at the intersection of clinical research, healthcare technology, and site enablement. Your core mission is to expand access to clinical trials by embedding research capabilities directly into everyday clinical care, particularly within community-based and specialty practices.
Key characteristics of the organization include:
- Technology-enabled clinical research infrastructure that integrates with electronic health records (EHRs) to identify potentially eligible trial participants using advanced analytics and machine learning.
- A focus on bringing clinical trials into real-world care settings, rather than relying solely on large academic medical centers.
- Emphasis on patient access, physician empowerment, and data security, with systems designed to be HIPAA-compliant and audit-ready.
- Close collaboration with sponsors, CROs, and healthcare providers to support site operations, patient recruitment, and study execution at scale.
- Participant identification, screening, and recruitment, often leveraging technology-driven patient matching tools integrated with clinical workflows.
- Managing the informed consent process, ensuring participants understand study requirements and that documentation meets regulatory and IRB standards.
- Coordinating and conducting study visits, including scheduling procedures, collecting source data, and ensuring protocol adherence.
- Entering and maintaining accurate data in electronic data capture (EDC), CTMS, and other digital research systems.
FAQs
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