Cardiology Clinical Research Coordinator I: Impactful Trials

MedStar Health’s Washington Hospital Center; Washington (District of Columbia); Hybrid; USD 49,000 - 87,000; Full time

Job summary

MedStar Health’s Washington Hospital Center is seeking a Clinical Research Coordinator I to support a portfolio of studies under moderate supervision. Responsibilities include IRB submissions, regulatory coordination, and data entry into CTMS.

The role involves pre-screening and enrolling participants, consent, and ensuring regulatory compliance. Required are 1–2 years of clinical research experience and a high school diploma or GED; a Bachelor’s degree or allied health degree is preferred.

Qualifications

• High School Diploma or GED required; bachelor’s degree or allied health degree preferred.
• 1–2 years of relevant clinical research experience or equivalent.
• Healthcare setting experience preferred.

Responsibilities

• Assist IRB submissions and regulatory forms; coordinate essential regulatory documents.
• Participate in the informed consent process of research participants.
• Pre-screen, screen, and enroll potential research participants.
• Maintain study source documents and data entry in CTMS; address queries in real time.

Skills

Verbal communication

Written communication

Basic computer skills

Education

Bachelor's degree or allied health degree preferred

Tools

CTMS

Job description

MedStar Health’s Washington Hospital Center is seeking a Clinical Research Coordinator I to support a portfolio of studies under moderate supervision. Responsibilities include IRB submissions, regulatory coordination, and data entry into CTMS.

The role involves pre-screening and enrolling participants, consent, and ensuring regulatory compliance. Required are 1–2 years of clinical research experience and a high school diploma or GED; a Bachelor’s degree or allied health degree is preferred.