- Lilly (Indianapolis, IN)
- …and Development (PRD) Quality Assurance ( QA ) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA CT ... stability justifications and retest dating for clinical trial (CT) Materials. + Provide Quality oversight for Collaboration Partners as needed. + Assist with… more
- Actalent (Remote, OR)
- …Compliance + EU CTR + US FDA + ICH GCP + Clinical Protocol + Quality Assurance + CTIS + Trial Disclosure Additional Skills & Qualifications + Bachelor's ... We are seeking a dedicated Trial Disclosure Associate to support clinical trial ...meet project objectives. Responsibilities + Support clinical trial applications via CTIS by uploading and quality… more
- Actalent (Frederick, MD)
- …The ideal candidate will be a highly motivated professional who can oversee Quality Assurance clinical operations. The Associate Director of QA will ... late stage/commercial cell therapy products. Principal Duties/Responsibilities: * Leads Quality Assurance ( QA ) oversight for...in biopharmaceutical quality assurance and clinical quality assurance . * In-depth… more
- Lilly (Indianapolis, IN)
- …of the medicines needed for clinical trials (CT). As Foundry Computer Systems Quality Assurance (CSQA) Associate , you will be responsible for the ... reducing costs and environmental impact. The Lilly Medicine Foundry Quality Assurance ( QA ) supports the...variety of other systems that enable clinical trial supply. **Responsibilities** As a Foundry CSQA Associate… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …on site in Silver Spring, Maryland. Responsible for all onsite Clinical Trial activities involving quality assurance and compliance with applicable ... Responsible for Quality Assurance /Regulatory Compliance of all onsite Clinical Trial activities + Conducts audits and reviews/analyzes data and… more
- Lilly (Greenwood, IN)
- …responsible for quality support for the Greenwoon Innovation Center (GIC). The QA Associate will drive large-scale quality improvement projects and ... for GIC. The Associate and Advisor - QA PR&D Centralized Services and Supplies provide quality... quality oversight for Direct-to-Patient and other Decentralized Clinical Trial models. + Support and provide… more
- General Dynamics Information Technology (Fairfax, VA)
- …changes needed based on current project status. + Work with Clinical Quality Assurance to ensure trial compliance with applicable regulations (ICH-GCP, ... Trust/Other Required:** None **Job Family:** Science and Research **Skills:** Biotechnology, Clinical Quality Assurance , Clinical Research,Regulatory… more
- GRAIL (Durham, NC)
- …discipline (advanced degree preferred) + 10 + years relevant experience in clinical quality assurance , diagnostics, and/or regulatory compliance within ... into organizational processes. + Collaborate with cross-functional teams (eg, Regulatory, Quality Assurance , Lab Operations, Clinical Data Management,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ Establish metrics to evaluate training effectiveness and implement continuous improvement ** Clinical Quality Assurance & Compliance:** + Implement ... of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD)...maintain clinical SOPs and clinical trial related device documentation + Support quality … more
- Abbott (Alameda, CA)
- …members, peers, and management. + Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical ... implementation of clinical studies from concept to clinical study report per timelines and quality ...required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and… more