Senior Clinical Research Coordinator - Onsite (Houston)

Baylor College of Medicine; Houston (TX); On-site; USD 71,000 - 83,000; Full time

Job summary

Baylor College of Medicine in Houston, TX is seeking a Senior Research Coordinator in the Clinical Research Division to provide centralized coordination across multiple Principal Investigators and trials, including therapeutic drug and device studies.

This onsite role supports study activity with regulatory staff, sponsors, and the OCR team; requires a BS in Basic Science or related field and five years of experience, with occasional after-hours work as needed.

Qualifications

• Bachelor's degree in Basic Science or related field; four years of related experience may substitute for degree requirement.
• Five years of relevant experience.

Responsibilities

• Recruits, schedules and conducts daily activities of clinical research participants with investigators and regulatory staff.
• Attends staff meetings; provides training on regulations and best practices to new coordinators.
• Participates in study qualification, feasibility activities and close-out activities for report to research manager.
• Liaises with PI, Sponsor, Research Manager and OCR Research Finance to support all study activities.
• Supports timely reporting of study status, enrollment, monitoring, and site visits.
• Coordinates scheduling of pre-site and site initiation visits with Research Manager and PIs.
• Performs quality control reviews and chart reviews; completes data collection and database queries.
• Engages in cross-coverage across OCR study support as needed.

Skills

Coordination

Clinical research

Regulatory knowledge

Cross-functional teamwork

Education

Bachelor's degree in Basic Science or related field

Job description

Baylor College of Medicine in Houston, TX is seeking a Senior Research Coordinator in the Clinical Research Division to provide centralized coordination across multiple Principal Investigators and trials, including therapeutic drug and device studies.

This onsite role supports study activity with regulatory staff, sponsors, and the OCR team; requires a BS in Basic Science or related field and five years of experience, with occasional after-hours work as needed.