Edc Jobs

Celerion is hiring an EDC Test Analyst to perform UAT and validate clinical databases and systems to ensure compliant, timely study execution across clinical trials.

Celerion is hiring an EDC Database Developer to design and build eCRFs, program edit checks, and manage Veeva-based EDC deployments to support clinical trials across multiple studies.

Edwards Lifesciences seeks a Clinical Data Management Analyst to define EDC requirements, ensure clinical data quality, and support study operations for TMTT clinical trials in a hybrid Irvine-based role.

IQVIA is seeking a CRA 2 to perform site selection, initiation, monitoring, and close-out activities for early clinical development trials, primarily supporting Phase 1/2 studies.

Milestone One is hiring a hybrid Lead Site Coordinator to provide regional oversight, training, and operational support for clinical research sites across the Northeast and West Coast.

Rho seeks a motivated Clinical Data Associate to support EDC build, data cleaning, UAT validation, and basic SAS data review for clinical studies on the Federal Research Team.

Mid-level Clinical Research Coordinator to manage day-to-day study coordination, participant activities, specimen handling, and regulatory compliance at the University of Miami medical campus.

Senior leadership role to define and execute clinical data management strategy for Bicycle Therapeutics' oncology programs, overseeing internal teams, vendors, and regulatory-ready data delivery.

Georgetown University is hiring a part-time Data Analyst to support infectious disease clinical trials with data entry, validation, documentation and process improvement at its Medical Center.

WEP Clinical is hiring an Associate Clinical Data Manager to support end-to-end data management activities for clinical programs, ensuring accurate, compliant, and timely delivery of data products.

The Hematology/Oncology division at the University of Chicago seeks a Senior Clinical Research Data Manager to lead data management activities for complex oncology clinical trials and ensure data integrity across industry, investigator-initiated, and NCTN studies.

Lead the design, delivery, and standardization of clinical trial systems at AbbVie to optimize data flow, user experience, and regulatory compliance.

Faro Health is looking for an experienced Clinical Operations specialist to model and quality-check trials in the Faro Study Designer and support clinical solutions on a 5+ month remote contract.

Experienced clinical research professional needed to lead and manage complex clinical trials at Emory University's Georgia Clinical & Translational Science Alliance, ensuring regulatory compliance and high-quality data delivery.

SGS is seeking an entry-level Clinical Research Coordinator I to manage study activities, collect and record clinical data, and ensure compliance with protocols and GCP at its Richardson clinic.

Experienced or early-career clinical research professionals are invited to apply for an onsite Clinical Data Coordinator role supporting accurate CRF completion, query management, and specimen handling within Hackensack Meridian Health’s research teams.

Avera Research Institute is hiring a Clinical Research Coordinator to manage study operations, participant interactions, and data/specimen workflows for clinical trials in Sioux Falls.

AbbVie is hiring a Study Management Associate III in Mettawa, IL to support operational management of Investigator Initiated Studies and medical affairs research from intake through publication.

Celerion seeks a Clinical Study Manager I to manage on-site study execution, ensure quality and timelines, and support client relationships for early-phase clinical trials.

Experienced statistical programming manager needed to lead SAS-based dataset and output development, QC, and CRO oversight for clinical trials at REGENXBIO in Rockville, MD.

Lead site management and monitoring activities for clinical studies at Exact Sciences, ensuring protocol adherence, regulatory compliance, and strong sponsor-site relationships in a remote field-based role.

RQM+ seeks a Clinical Data Science Associate to support EDC setup, data monitoring, reconciliations, and TMF readiness for MedTech clinical studies in a remote role.

Part-time Biostatistician I (Colorado-based, remote) to support clinical trial design, SAS programming, and statistical analyses across therapeutic areas.