Clinical Research Coordinator II - Patient Trials

Houston Methodist; Houston (TX); On-site; USD 55,000 - 85,000; Full time

Job summary

Houston Methodist Academic Institute is seeking a Research Coordinator II to manage day-to-day activities of research protocols, assess patient qualification, and ensure accurate data collection and safety of participants. Under minimal supervision, you will coordinate data collection, prepare regulatory documents, obtain informed consent, and support study staff with essential administrative duties.

Qualifications include a Bachelor’s degree and four years of research experience; preferred

Qualifications

• Bachelor’s degree required.
• Four years of research experience.
• Licenses and certifications required

Responsibilities

• Coordinate day-to-day activities of research protocols.
• Identify and recruit clinical research subjects; monitor enrollment.
• Obtain informed consent and document data; collect vital signs as trained.
• Prepare IRB documents and assist with regulatory approvals.
• Maintain source documentation for quality and accuracy; support QA processes.
• Assist PI and staff with budget, regulatory and protocol-related tasks

Skills

Communication

Customer service

Independence

Analytical thinking

Attention to detail

Education

Bachelor’s degree

Job description

Houston Methodist Academic Institute is seeking a Research Coordinator II to manage day-to-day activities of research protocols, assess patient qualification, and ensure accurate data collection and safety of participants. Under minimal supervision, you will coordinate data collection, prepare regulatory documents, obtain informed consent, and support study staff with essential administrative duties.

Qualifications include a Bachelor’s degree and four years of research experience; preferred