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Job summary
A prominent health institution in Houston is seeking a Clinical Research Coordinator to support regulatory document preparation, recruit clinical trial subjects, and assist in staff education. The ideal candidate will have a Bachelor’s degree and four years of research experience, with certifications such as CCRC or CCRP preferred. Strong communication skills and the ability to work independently are essential. This role may include various essential functions related to quality assurance and financial management in clinical research.
Qualifications
Four years of research experience required.
CCRC or CCRP certifications preferred.
Demonstrates competencies for job performance.
Responsibilities
Draft communications for the Sponsor and regulatory documents.
Identify and recruit clinical research subjects.
Assist in educating research staff on scientific aspects.
Skills
Effective communication with patients and staff
Ability to work independently
Sound judgment and analytical skills
Proficiency in English
Education
Bachelor’s degree
Job description
A prominent health institution in Houston is seeking a Clinical Research Coordinator to support regulatory document preparation, recruit clinical trial subjects, and assist in staff education. The ideal candidate will have a Bachelor’s degree and four years of research experience, with certifications such as CCRC or CCRP preferred. Strong communication skills and the ability to work independently are essential. This role may include various essential functions related to quality assurance and financial management in clinical research.