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Medasource

Clinical Research Coordinator

Medasource, Washington, District of Columbia, United States


Clinical Research Coordinator 2 6 Month Contract-to-Hire Onsite in Washington, DC (remote flexibility once fully converted) Start Date: ASAP Job Description: The Clinical Research Coordinator II (CRC II) will support our Client's Research Institute in their Women's & Infant's Services research group to play a pivotal role in coordinating and managing clinical research studies. This position involves ensuring compliance with protocols, regulatory requirements, and organizational policies while supporting investigators and research teams to achieve study objectives. Responsibilities -Oversee clinical research projects, including study startup, implementation, monitoring, and closeout -Coordinate study activities with principal investigators, research teams, and external sponsors -Prepare and submit IRB applications, amendments, and continuing reviews -Ensure adherence to federal, state, and institutional regulations -Identify, screen, and recruit eligible participants for clinical trials -Obtain informed consent and ensure participant understanding of study procedures -Collect, document, and manage study data in compliance with protocol requirements -Utilize electronic data capture systems and resolve data queries in a timely manner -Assist in internal and external study monitoring and audits -Prepare and present progress reports, adverse event reports, and study updates -Serve as the primary point of contact for study sponsors, regulatory agencies, and research team members -Participate in team meetings, trainings, and quality improvement initiatives Required Qualifications: -Education: HS Degree minimum -3 years of experience in clinical research within a healthcare setting -Strong patient engagement experience -Experience with in-person study recruitment -Experience with administrative responsibilities associated with clinical research studies -Regulatory/compliance management, documentation, etc. Preferred Qualifications: -Women's Health research experience -Certifications/licensure such as CCRC, CCRP, etc. are a plus