Clinical Data Manager - Temp to Perm
 The Emmes Company, LLC | |
 United States, Maryland, Rockville | |
 May 13, 2026 | |
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Overview
Clinical Data Manager - Temp to Perm US - Remote Note for Applicants: This assignment will start you off as a temporary full-time employee working 40 hours per week. The work presently is forecasted to go till December 31, 2026. (As new data becomes available, this forecast may change.) And after that, a decision will be made if the work will continue and if so, whether or not to convert whomever is in the role to a FTE. Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Data Manager is responsible for data management activities for research studies. The Data Manager works as an integral part of a cross-functional team through the lifecycle of the research study from design through final analysis and study closeout. The Data Manager is responsible for the completeness and accuracy of the study data in the electronic database and collaborates with internal and external project teams on all aspects of data collection. Responsibilities * Participates with cross-functional teams in design, documentation, testing, and implementation of clinical data collection studies in an electronic data capture (EDC) system * Designs and/or develops study-specific electronic or paper Case Report Forms (CRFs), ensuring consistency with study protocol, clinical requirements, and accurate and efficient data collection * Collaborates with the project team and other study personnel to determine data collection requirements based on the study protocol and system knowledge * Documents and resolves data management issues for a protocol or group of protocols * Assists with communication for internal and external teams to resolve data management issues * Creates or reviews data validation check specifications; coordinates with relevant parties in the development and testing of eCRF and data validation checks * Helps organize project team meetings and facilitates efficient project communication to ensure deadlines are met; participates in department meetings * Creates and maintains study data management documents according to instructions (e.g. Data Management Handbook, Data Management Plan, Data Validation Plan, EDC System User's Guide, EDC Training and Certification Documents) * Prepares data reports and assists with data presentations as applicable * Reviews data obtained through Electronic Medical Records (EMR) integration, commercially available EDC systems, or other external data sources * Mentors assigned employees on data management procedures and guidelines * Identifies and resolves data queries and discrepancies; contributes to data quality metrics for a protocol or project; conducts data quality audits * Conducts training for users on the EDC system and protocol-specific EDC requirements; maintains training documentation and manages system user access * Other duties as assigned Qualifications
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