Clinical Research Coordinator II

We are recruiting for several experienced Clinical Research Coordinators to join our MedStar Health Research Institute teams in Washington, D.C. to implement and coordinate research and administrative procedures for the successful management of clinical trials. Perform diverse administrative duties requiring analysis, sound judgment and a high level of knowledge of study specific protocols.

What you will do

• Coordinate clinical trials: Manage day-to-day study activities from start-up through close-out, ensuring compliance with protocols, sponsor requirements, and institutional policies.

• Support research participants: Lead recruitment and informed consent, coordinate study visits and assessments, answer participant questions, and promote participant safety throughout the study.

• Manage regulatory requirements: Coordinate IRB submissions, study documentation, delegation of responsibilities, adverse event reporting, and other regulatory requirements.

• Maintain study data: Complete accurate clinical documentation and case report forms, enter data into the CTMS within required timelines, and resolve data queries with sponsors/CROs.

• Coordinate study procedures and supplies: Oversee laboratory testing, biospecimen handling, investigational product accountability, equipment requirements, and other protocol-specific activities.

• Collaborate across teams: Serve as a liaison among participants, investigators, sponsors, CROs, and healthcare professionals while supporting study monitoring, initiation, and close-out visits.

Qualifications

• Bachelor's degree or an allied health or related professional degree required, or equivalent work experience required
• 2 years of relevant clinical research experience required
• Experience in a healthcare setting preferred
• Undergraduate and/or work experiences that demonstrate aptitude for research facilitation preferred
• Verbal and written communication skills
• Basic computer skills preferred