- Regeneron Pharmaceuticals (Armonk, NY)
- …to help shape how regulated processes are managed across Global Development. As Manager , GDQTC, you'll support our Veeva Quality Suite-based eQMS _which manages ... investigations-within a GCP or GVP setting. Experience with the Veeva Quality Suite (especially QualityDocs and QMS modules) is strongly preferred, and formal… more
- PCI Pharma Services (Rockford, IL)
- …to pioneer and shape the future of PCI. n Job Description **Commercial Associate Project Manager ** Assists with designated execution of customer projects and ... to the customer (as required). + Work with Incoming Quality Department to ensure timely release of components and...for customer owned inventory. Provide continuous support to Project Manager and team for day-to-day internal problem solving and… more
- Lockheed Martin (Fort Worth, TX)
- …Be Doing** The Operations Systems & Modeling AI team is seeking an experienced manager to lead the AI for Operations portfolio\. You will set strategic direction, ... development, testing, and deployment of scalable AI solutions; ensure code quality , security, and maintainability\. * Stakeholder & Change Management - Partner… more
- Deloitte (New York, NY)
- …(iCRS) group within Deloitte's International Tax practice. What you'll do As a Tax Manager , you will work within an engagement team and draw on experience in ... Certified Business Analysis Professional + Certified SAFe Lean Portfolio Manager + Certified SAFe Architect + Certified SAFe Agile...Lifecycle Professional (CSSLP) + ASQ - American Society for Quality - Software Quality Engineer + SEI… more
- Parexel (Richmond, VA)
- …with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential ... (CSP) or ICH- GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. + Assists site in maintaining inspection ready ISF.… more
- Parexel (Columbus, OH)
- …with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential ... The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery...GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. + Assists site in… more
- Parexel (Austin, TX)
- …to safeguard the quality of investigator sites (eg patient safety, site quality and compliance with GCP ), to maintain investigator and site staff engagement ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws,… more
- Abbott (Minneapolis, MN)
- …with diabetes from routine fingersticks. Summary Under the supervision of senior colleague/ manager (or delegate), the Associate Clinical Site Lead drives study ... and follow-ups when indicated (or ensure trained personnel attend). + Regulatory and Quality + Strong understanding of GCP and commitment to progress knowledge… more
- IQVIA (Carlsbad, CA)
- …documents for all relevant site personnel within agreed timelines (eg, FD, CV, GCP certificates, DSL, etc.) Supports the SSU Manager with preparation of ... country in accordance with monitoring procedures and processes following ICH/ GCP , local regulations and SOPs. Proactive site preparation and...SSO Study Start-Up Team Lead, the SSO Study Start-Up Manager , and the SSO Feasibility Manager as… more
- ThermoFisher Scientific (Las Vegas, NV)
- …includes a drug screening. Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is an ... office-based position for a motivated Physician. The Associate Medical Director serves as the physician investigator on all assigned clinical trials providing… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- … Associate . * Extensive knowledge of trial oversight activities, GCP /ICH and federal regulations, IRB/EC and Investigator responsibilities. * Familiarity with ... clinical studies at the site level ensuring adherence to protocols, timelines, ICH/ GCP guidelines, and federal regulations. The Sr CRA will perform site… more
- Capital One (Mclean, VA)
- Associate , Cyber Risk & Analysis - Enterprise Services Risk The Enterprise Services Risk organization is expanding with a focus on attracting innovative, pioneering, ... we work to redefine the financial sector. As an Associate on the Enterprise Services Controls Governance team, you...changes obtain appropriate approvals + Monitor metrics around data quality to ensure control data is complete and accurate… more
- University of Southern California (San Diego, CA)
- …Disease (AD) through innovative clinical trials. Key Responsibilities: + Data Quality Assessment: Identifying, assessing, and resolving data quality problems ... until queries are properly closed to ensure it meets quality standards and objectives. Performs external & internal labs...with the clinical team such as the CRAs, Project Manager , Analytical Developers, Lead Data Managers, clinical sites and… more
- ThermoFisher Scientific (Suwanee, GA)
- …digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities ... clients define and develop clinical programs, minimize delays, and execute high- quality , cost-efficient clinical studies. Our Clinical Operations team within the PPD… more
- ThermoFisher Scientific (Carlsbad, CA)
- …digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities ... procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and… more
- ThermoFisher Scientific (West Hills, CA)
- …digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities ... Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study… more
- Taiho Oncology (Princeton, NJ)
- …of a dynamic team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support during study start-up, ... Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies. + Updates...+ Monitors Trial Master File related KPIs and performs quality review of the eTMF (per CRO oversight plan)… more
- Terumo Neuro (Aliso Viejo, CA)
- …Monitoring Plans in collaboration with a Project Manager and Clinical Quality Assurance. + Assume Lead Clinical Research Associate responsibilities on ... **12869BR** **Title:** Sr Associate , Field Clinical Monitoring (US Remote) **Job Description:**...of delivering start-up goals, enrollment targets, and required data quality . + Facilitate and maintain open communication among investigational… more
- Walmart (Bentonville, AR)
- …** **What you'll do ** Join Walmart as **Senior, Software Engineer - Associate Digital Communication** in our Global Technology EBS team. Your work could help ... the Team** This team develops dynamic front-end experiences for an associate facing digital signage communications platform, collaborating closely with corporate… more
- ManpowerGroup (Sunnyvale, CA)
- **Title:** Clinical Research Associate (CRA) **Location:** Sunnyvale, CA **Duration:** 12 Months **Pay Range:** $45 to $50/hr We are looking for an **Internal ... Clinical Research Associate (CRA)** to join one of our growing Clinical...lifecycle-from start-up to close-out-under the supervision of the Clinical Manager . The role involves conducting qualification, initiation, monitoring, and… more