Associate, Clinical Data Management (RID00216)
Full-time
US
Oct 25, 2026
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About the Role
Associate / Senior Associate, Clinical Data Management Clinical Research | SS&A Are you passionate about clinical data quality and the future of patient-centered research? We're looking for an Associate / Senior Associate, Clinical Data Management to support the delivery and oversight of clinical and patient-reported data within EDC platforms, including our innovative iTakeControl (iTC) technology. You'll work across clinical operations, product, and technical teams while supporting studies from startup through closeout. Experience Level: 0-10 years Required Qualifications Undergraduate degree or equivalent professional experience Experience supporting clinical study protocols, protocol amendments, observational research, registries, data migrations, reporting, and data transfers Professional experience within biopharma, pharmaceutical, CRO, clinical site, or consulting environments Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, FDA 21 CFR Part 11, Annex 11, and GxP processes Experience with or understanding of EDC, ePRO, EHR, clinical research technologies, and health data collection systems Experience managing multiple projects, timelines, stakeholders, vendors, and study teams simultaneously Strong written and verbal communication skills with proficiency in Microsoft Office (Word, Excel, PowerPoint) What You'll Do Manage and review clinical and ePRO data, including video-based data collection Develop Data Management Plans, CRF Specifications, eCRFs, and study do