Clinical Research Coordinator II – Patient-Centric Trials

Houston Methodist; Houston (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Houston Methodist is seeking a Research Coordinator II to manage day-to-day activities of clinical research protocols, assess patient eligibility for studies, and ensure accurate data collection, documentation, and safety of participants under minimal supervision.

You will gather patient data for clinical research per the study protocol and support study-related administration, coordinating with investigators and maintaining regulatory documentation.

Qualifications

• Bachelor's degree required.
• At least four years of research experience.
• CCRC or CCRP preferred (certifications from ACRP/SOCRA).
• Demonstrates safe research practices and data integrity.

Responsibilities

• Drafts communications with Sponsors and regulatory documents.
• Identifies and recruits clinical research subjects and monitors enrollment goals.
• Obtains informed consent and documents appropriately; supports site visits.
• Maintains source documentation and QA processes for accuracy and compliance.

Skills

Communication skills

English proficiency

Independent worker

Judgment & analytics

Customer service focus

Education

Bachelor's degree

Job description

Houston Methodist is seeking a Research Coordinator II to manage day-to-day activities of clinical research protocols, assess patient eligibility for studies, and ensure accurate data collection, documentation, and safety of participants under minimal supervision.

You will gather patient data for clinical research per the study protocol and support study-related administration, coordinating with investigators and maintaining regulatory documentation.