Research Coordinator

IQVIA seeks a Research Coordinator to support clinical trial operations in Houston or Austin. The role encompasses patient screening and enrollment, protocol compliance monitoring, informed consent facilitation, and clinical trial data management while ensuring patient safety and regulatory adherence.

Responsibilities Screen and enroll eligible patients while managing informed consent discussions and documentation Coordinate protocol-required patient visits, procedures, and study activities according to timelines Monitor protocol compliance, adverse events, and deviations; report to sponsors and IRB as needed Abstract clinical data from source documents and enter into case report forms accurately Assess patient adherence to study requirements and address barriers to participation Requirements Knowledge of clinical research regulations, GCP guidelines, and IRB processes Experience with informed consent procedures and patient education Proficiency in electronic data capture systems and CRF completion Strong documentation and attention to detail in medical records Ability to communicate effectively with interdisciplinary clinical teams Understanding of oncology clinical trial protocols and study procedures