Clinical Research Coordinator

Company: Mid-Atlantic Nephrology Associates PA
Location: Windsor Mill
Posted on: April 3, 2026

Job Description:

Large nephrology practice in Baltimore seeks a Clinical Research Coordinator to be responsible for coordination of all aspects of assigned clinical trials from pre-study planning through successful completion of all patient/subject visits and study documentation; directly involved in patient/subject care and study subject’s procedures and activities. Purpose and Scope: The Clinical Research Coordinator (CRC) for the nephrology practice is responsible for overseeing all aspects of clinical research studies, ensuring compliance with regulatory standards, and facilitating the conduct of the study. Responsibilities include : • Collect study data by recruiting and coordinating activities of study participants. • Utilize a basic understanding of the clinical study background and rationale to explain. the study to potential and current participants. • Responsible for patient enrollment, verify patient conformity to inclusion/exclusion criteria prior to patient enrollment in the study. • Assist in developing recruitment strategies for one or more studies. • Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for patient/subject visits, obtaining informed consent, visit schedules, tests, procedures, laboratory information, and drug accountability requirements. • Set up tools and procedures for data collection and study processes. • Perform data entry and organize data in approved systems. • Serve as liaison between study team and IRB for routine administrative matters. • Prepare routine reports related to study accrual, study trends, efficiency-related issues. • Contact participants to confirm, schedule, and retain. • Responsible for all study documentation forms. • Other duties as assigned. Job Summary and Qualifications • Must be proficient with computers, Microsoft Office applications and Windows operating systems. • Ability to communicate and maintain effective interpersonal relations at various levels of the organization. • Strong organizational and communication skills • This role may require some travel to various locations approximately 20% of the time. • High School diploma or graduation equivalent. • 1-year of related experience preferred. • 1-2 years of clinical trials/research experience are preferred. PHYSICAL DEMANDS AND WORKING CONDITIONS: • The physical demands and work environmental characteristics described here are representative of those an employee encounters while performing the essential functions of this job. • Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. • Day-to-day work includes desk and personal computer work and interaction with patients, patient families, facility staff, physicians, and the community at large. We offer a competitive salary commensurate with experience and a robust benefit package including health, dental, vision, Short Term Disability, Long Term Disability, Group Term Life, PTO, paid holidays, and 401(k) plan with generous employer contribution. Prospective employees must pass a criminal background check and provide proof of Influenza Vaccination including booster. View all jobs at this company

Keywords: Mid-Atlantic Nephrology Associates PA, Sterling , Clinical Research Coordinator, Healthcare , Windsor Mill, Virginia