- IQVIA (Overland Park, KS)
- …Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
- Avania (OR)
- …for the key role of experienced Clinical Research Associate (CRA) or Senior Clinical Research Associate ( Sr CRA) As a CRA/ Sr CRA you will be ... for several studies running in parallel, in all associated clinical trial phases, from regulatory submissions to...3 + years of relevant work experience as a clinical research associate - CRA. + Attention… more
- United Therapeutics (Research Triangle Park, NC)
- …disease process, and lead protocol development and writing. **Minimum Requirements** + For Senior Clinical Drug Development Scientist level: + 10+ years of ... + Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, external… more
- BeOne Medicines (Emeryville, CA)
- …with CRAs to ensure data collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to ... Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a thorough knowledge of ICH and… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... IQVIA Biotech is hiring for our Early Clinical Development team. Ideal candidates will have Phase...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Lilly (Indianapolis, IN)
- …4. Scientific Data Dissemination and Exchange + Ensures timely dissemination of clinical trial data. + Help to ensure the critical analysis ... Senior Director-Medical is delegated various responsibilities by the Associate Vice-president or equivalent role to provide leadership, supervision, coordination,… more
- Amgen (Washington, DC)
- …of, and QC study-related documents (eg study concept documents and protocols). Interpret clinical trial data and participate in safety assessments. Review and ... time for a career you can be proud of. ** Clinical Research Sr Medical Scientist, Endocrinology -...scientific and practical rationale + Familiarity with concepts of clinical research and clinical trial … more
- J&J Family of Companies (Cambridge, MA)
- …disease area and/or pathway strategies. They will be empowered to lead a cross-functional clinical trial team to deliver on the trial 's major execution ... We are searching for the best talent for an Associate Director, Translational Medicine Clinical Lead, Translational...study of immunologic disease, immunologic pathways, and in early clinical trial design and execution. TS has… more
- Abbott (Abbott Park, IL)
- …and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Senior Clinical Site Lead** Summary The Senior Clinical ... (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and ...competent authority/ethics committee. Beyond developing and maintaining a productive clinical territory, the Senior Clinical … more