Oncology Clinical Trials Coordinator III – Phase I (Houston)

Baylor College of Medicine; Houston (TX); On-site; USD 57,000 - 67,000; Full time

Job summary

Baylor College of Medicine in Houston, TX is seeking a Research Coordinator III for Duncan Cancer Center to manage oncology clinical trials. The role covers screening, enrollment, data collection, and safety reporting to regulatory bodies, working closely with senior staff.

The position is onsite, with responsibilities extending to adverse event assessment, collaboration with physicians, and ensuring adherence to GCP guidelines while coordinating with clinic and hospital staff to maintain

Qualifications

• Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
• Two years of relevant experience.

Responsibilities

• Coordinates day-to-day activities of research protocols, including screening, enrollment, and monitoring of research participants.
• Ensures accurate data collection, documentation, organization, and the safety of research participants.
• May supervise other research staff.
• Coordinates assignments involving research specialties, clinic staff, and hospital staff to ensure protocol adherence and that studies are conducted in accordance with Good Clinical Practice (GCP) guidelines.
• Maintains daily coordination activities while working to minimize clinic visits and complete study procedures in a manner that does not interfere with routine clinical care.
• Conducts comprehensive assessments of adverse events in collaboration with the participant's physician and other care team members.
• Reports adverse events to the sponsor and communicates necessary modifications to the treating physician.
• Serves as the primary point of contact for clinical trial participants and assesses potential impact on study conduct.

Education

Bachelor's degree in a related field

Two years of relevant experience

Job description

Baylor College of Medicine in Houston, TX is seeking a Research Coordinator III for Duncan Cancer Center to manage oncology clinical trials. The role covers screening, enrollment, data collection, and safety reporting to regulatory bodies, working closely with senior staff.

The position is onsite, with responsibilities extending to adverse event assessment, collaboration with physicians, and ensuring adherence to GCP guidelines while coordinating with clinic and hospital staff to maintain