Associate Clinical Data Manager

Overview

Associate Clinical Data Manager

Location: Remote

Be Part of One Team, One Purpose.

At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.

Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.

We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.

The Associate Data Manager is responsible for assisting with data management activities for research studies. The Associate 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 Associate Data Manager is responsible for the completeness and accuracy of the study data in the electronic database and collaborates primarily with internal project teams on all aspects of data collection.

Responsibilities

• Assists cross functional teams with the documentation, testing, and implementation of clinical data collection studies in an electronic data capture EDC system.
• Contributes to design and/or development of study specific electronic or paper Case Report Forms (CRFs), utilizing study protocol and clinical requirements.
• Assists the project team and other study personnel to determine data collection requirements based on the study protocol.
• Assists with documenting and resolving data management issues in conjunction with the DM team.
• Assists with review, implementation, and evaluation of data validation processes, example, edit checks.
• Utilizes study data management documents, example, Data Management Handbook, Data Management Plan, Data Validation Plan, EDC System User's Guide, EDC Training and Certification Documents.
• Assists with reviewing data obtained through Electronic Medical Records EMR integration, EDC systems, or other external data sources.
• Attends and participates in project and department meetings as required.
• Assists with identification and resolution of data queries and discrepancies, assists with data quality audits.
• Assists with training users on the EDC system and protocol specific EDC requirements, maintains related training documentation and supports system user access.
• Assists with preparation of data reports as applicable.
• Performs other duties as assigned
• Complies with all policies and standards

Qualifications

• Bachelor's Degree Public health, clinical, science, technical, or related discipline; equivalent combination of education and relevant work experience may be considered in lieu of a degree Required
• 1-3 years of experience in clinical data management, electronic data capture (EDC), or related clinical research role. Required
• less than 1 year Experience assisting in the design, development, and implementation of study-specific CRFs (electronic or paper). Preferred
• less than 1 year Familiarity with clinical study protocols, data validation processes, and query resolution. Preferred
• less than 1 year Exposure to cross-functional team collaboration in clinical research settings. Preferred
• less than 1 year Experience with reviewing data from EMR integration, EDC systems, or other external data sources. Preferred
• less than 1 year Basic experience providing training and support for EDC users and documenting related activities. Preferred
• less than 1 year Knowledge of study data reporting, quality audits, and adherence to regulatory and SOP standards. Preferred
• Excellent verbal and written communication skills High
• Skills in prioritization, organization, and time management High
• Strong attention to detail, adaptable, and flexible High
• Knowledge of Microsoft Office suite is essential High

If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.

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