Cancer Clinical Trials Research Coordinator I

Houston Methodist; Houston (TX); On-site; USD 52,000 - 76,000; Full time

Job summary

Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility, and ensure accurate data collection and safety of participants. This role supports documentation and collaboration within the care and research teams in a fast-paced clinical environment.

Responsibilities include screening patients, scheduling tests, maintaining regulatory records, and contributing to data integrity and study quality while following ICH/GCP

Qualifications

• Bachelor’s degree required.
• Two years’ research experience required.
• Demonstrates strong data entry and documentation skills.
• Excellent communication with patients, physicians and staff.
• Ability to apply judgment and analytical thinking.

Responsibilities

• Screen patients to evaluate eligibility for studies.
• Coordinate scheduling of subject appointments and tests.
• Enter accurate data into source documents and electronic systems.
• Maintain records for clinical study and regulatory documents.
• Report adverse events to regulatory authorities as required.

Skills

Clinical data entry

English proficiency

Communication skills

Analytical thinking

Judgment

Team collaboration

Education

Bachelor’s degree

Job description

Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility, and ensure accurate data collection and safety of participants. This role supports documentation and collaboration within the care and research teams in a fast-paced clinical environment.

Responsibilities include screening patients, scheduling tests, maintaining regulatory records, and contributing to data integrity and study quality while following ICH/GCP