The Clinical Research Coordinator organizes, coordinates, and implements research studies for the Penn Pregnancy & Perinatal Research Center. The role is responsible for study coordination, including participant recruitment, data entry and management, biospecimen collection, participant visits and follow-up, and regulatory documentation. The position is contingent upon continued funding. The Clinical Research Coordinator A performs study eligibility screening and consent across multiple studies; works with the clinical team to support positive participant encounters; provides protocol-required clinical services, including phlebotomy and biospecimen collection; handles participant calls and protocol-required telephone follow-up; maintains study data, source documents, case report forms, and individual patient records; responds to database queries and chart reviews; and works with community partners to support recruitment and retention. In addition to the A responsibilities, the Clinical Research Coordinator B coordinates participant visit schedules with study investigators and nurse practitioners, ensures that required tests and assessments are completed at each visit, reports adverse events and ensures investigator review and appropriate follow-up, and prepares detailed documentation of study activities. The candidate should be motivated and articulate, communicate effectively in writing and orally, work independently and collaboratively, and have strong planning, organizational, prioritization, and problem-solving abilities. Both levels require a bachelor's degree and the specified related experience in research and clinical study methodologies, or an equivalent combination of education and experience, and the ability to work flexible hours.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level