Clinical Research Coordinator I: Study Operations

Houston Methodist; Houston (TX); On-site; USD 55,000 - 70,000; Full time

Job summary

Houston Methodist is seeking a Research Coordinator to oversee day-to-day activities of research protocols and assess patient eligibility for studies. You will ensure accurate data collection, documentation, and safety of participants while supporting the research team.

The role requires a Bachelor’s degree and at least two years of research experience, with strong communication and data-entry skills to support high-quality study conduct and regulatory compliance.

Qualifications

• Bachelor’s degree required.
• Two years of research experience required.
• Strong data entry and documentation skills.
• Ability to communicate clearly with patients and staff.
• Capable of handling challenging situations with sound judgment.

Responsibilities

• Screen and interview to evaluate patient eligibility for studies.
• Coordinate daily activities of research protocols and data collection.
• Ensure accurate documentation in Source Documents, CRFs, and EDC systems.
• Schedule subject visits and coordinate tests/procedures.
• Maintain regulatory documents and report adverse events as needed.
• Collaborate with the care team to support study goals and safety.

Skills

Documentation and data entry

Clinical communication

Customer service oriented

Analytical thinking

Safety and compliance

Team collaboration

Education

Bachelor’s degree

Job description

Houston Methodist is seeking a Research Coordinator to oversee day-to-day activities of research protocols and assess patient eligibility for studies. You will ensure accurate data collection, documentation, and safety of participants while supporting the research team.

The role requires a Bachelor’s degree and at least two years of research experience, with strong communication and data-entry skills to support high-quality study conduct and regulatory compliance.