What are the responsibilities and job description for the Clinical Research Coordinator position at Halo Clinical Research?
Company Description
HALO Clinical Research is a physician-embedded Site Management Organization (SMO) that integrates clinical trials into established medical practices. By providing trained research staff, study equipment, regulatory oversight, and operational support, HALO enables physicians to conduct high-quality clinical research without the need for a standalone research site. The organization ensures studies are patient-focused, compliant, and maintain data integrity. HALO is dedicated to delivering exceptional clinical research through transparent partnerships and operational excellence.
Role Description
This is a full-time, on-site role for a Clinical Research Coordinator based in Houston, TX. The Clinical Research Coordinator will oversee the day-to-day implementation and coordination of clinical trials. Responsibilities include managing informed consent processes, adhering to protocol requirements, ensuring compliance with regulatory standards, and maintaining accurate documentation throughout the research process. The coordinator plays a pivotal role in supporting physicians and ensuring high-quality, patient-centered research outcomes.
Qualifications
- Experience with Informed Consent processes and ensuring patient understanding and compliance
- Knowledge of study Protocol adherence and its application in clinical research settings
- Proficient in conducting and managing Clinical Research and Clinical Trials
- Strong understanding of Clinical Research Experience and workflows
- Excellent organizational and documentation skills to maintain data integrity and regulatory compliance
- Bachelor’s degree in health sciences or a related field preferred
- Certification as a Clinical Research Coordinator (CCRC) is a plus
- Ability to work collaboratively with physicians and other healthcare professionals