Clinical Research Coordinator II

MedStar Health; Washington (District of Columbia); On-site; USD 60,000 - 102,000; Full time

Job summary

MedStar Health Research Institute in Washington, D.C. is recruiting several experienced Clinical Research Coordinators to implement and coordinate research and administrative procedures for successful clinical trial management.

You will perform diverse duties requiring analysis, sound judgment, and knowledge of study protocols. Responsibilities include coordinating trials from start-up to close-out, leading recruitment and informed consent, managing regulatory submissions, maintaining study data

Qualifications

• Bachelor's degree or allied health/related degree or equivalent work experience.
• At least 2 years of clinical research experience.
• Healthcare setting experience preferred.
• Undergraduate/work experience showing aptitude for research facilitation.
• Strong verbal and written communication skills.
• Basic computer skills preferred.

Responsibilities

• Coordinate clinical trials from start-up through close-out with protocol/sponsor compliance.
• Lead recruitment and informed consent, coordinate visits and assessments, support safety.
• Coordinate IRB submissions, study docs, delegation, and adverse event reporting.
• Maintain accurate study data and enter into the CTMS within timelines.
• Oversee laboratory testing, biospecimen handling, and equipment/supplies per protocol.
• Collaborate across teams with participants, investigators, sponsors, CROs, and healthcare pros.

Skills

Verbal communication

Written communication

Basic computer skills

Education

Bachelor's degree or allied health degree

Tools

CTMS

Job description

About the Job

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

This position has a hiring range of USD $59,820.00 - USD $101,836.00 /Yr.