This position will support funded research projects related to cardiovascular for the Pregnancy & Perinatal Research Center under supervision of the Director of Clinical Research Operations. The primary role of this position is the organization, coordination, and implementation of multiple clinical research studies. The essential functions of the position include but are not limited to: Develop and implement new/current study protocol design, construction of source documents, databases, and case report forms. Present monthly study updates at meetings. Assist with data cleaning and quality control for large volume interim analysis. Preparation and maintenance of regulatory documents including continuing reviews, modifications, and regulatory binders. Responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data entry, subject visits and follow-up and regulatory documentation. Work with Director of Clinical Research Operations to plan and lay groundwork for upcoming studies. Provide clinical services, including phlebotomy and biospecimen processing at patient visits, and be able to train on such processes. Actively troubleshoot and work as a problem solver in a large volume clinical setting to ensure full execution of protocols. Will participate in regulatory audits. Knowledge of pregnancy, preterm birth, and medical charts is required. Working and facile knowledge of RedCap and Excel are required. Prior experience with multi-site clinical trials is preferred.
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Job Type
Full-time
Career Level
Mid Level