- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- … Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ... IVRS set-up, central lab set-up, and other vendor selection processes. + Maintaining clinical trial management system (CTMS) information pertaining to the study… more
- ICON Clinical Research (Naperville, IL)
- …a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple ... Senior Clinical Research Associate ICON plc is...and site management, with proficiency in relevant clinical trial software and tools. + Excellent… more
- IQVIA (Boston, MA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures...activities from start-up to close-out. + Escalate and resolve trial issues and contribute to CAPA processes. ** Site… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- ThermoFisher Scientific (Suwanee, GA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
- Parexel (Atlanta, GA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …or related discipline. * 6+ years' experience as a Clinical Research Associate . * Extensive knowledge of trial oversight activities, GCP/ICH and federal ... site . * Serves as point of escalation for clinical site management and investigator sites. Liaises...contracted CRAs. * Supports the maintenance of documentation to clinical systems ( Clinical Trial Management… more
- AbbVie (Oregon City, OR)
- …of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data ... staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment...+ Ensures audit and regulatory inspection readiness at assigned clinical site at all times. + Manages… more
- Taiho Oncology (Princeton, NJ)
- …biological sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- Boehringer Ingelheim (Athens, GA)
- **Description** The Principal Clinical Research Associate will manage a team of Clinical Research Associates (CRA) that assist the Clinical Scientists ... site and in-house monitoring to verify that reported study/ trial data are accurate, complete, and verifiable from source...organization), conduct and reporting of on- site and off- site (national and global) clinical studies for… more
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