- Abbott (Alameda, CA)
- …serve people in more than 160 countries. **The Opportunity** : The Associate Clinical Project Manager is responsible for managing and meeting the objectives ... of clinical projects. Internally interfaces with data management, biostatistics, regulatory , clinical research associates, Finance, field clinical specialists, and… more
- Providence (Irvine, CA)
- …+ Assist in creating presentations and summaries for ongoing legal education on regulatory changes. + Draft and review legal documents to ensure compliance ... the future? Join Providence St. Joseph Health as our Associate Counsel and become a key player in shaping...legal guidance to PSJH's corporate and community Boards. + Review and draft routine contracts independently and offer advice… more
- Kelly Services (Sacramento, CA)
- Kelly(R) Science & Clinical is seeking a Quality Assurance Associate for a direct hire opportunity with a leading specialty pharmaceutical company at their R&D ... industries. **Workplace:** Onsite in Sacramento, CA. **Position Title:** Quality Assurance Associate **Position Type:** Direct hire **Pay rate:** $25-35 per hour. As… more
- Cedars-Sinai (Los Angeles, CA)
- …or contact for long term follow-up research participants only. *Assists with regulatory submissions to the Institutional Review Board (IRB) and works ... nationally for excellence in research!** **Job Responsibilities** The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research… more
- Cedars-Sinai (Los Angeles, CA)
- …contact or patient contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely ... nationally for excellence in research!** **Job Summary:** The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program… more
- MUFG (Los Angeles, CA)
- …+ Perform ongoing credit reviews of individual accounts through regular/ad-hoc credit review process and closely monitoring existing Problem Loans and Watch List ... lines and coordinate appropriate renewal. + Ensure compliance with external regulatory /internal policy and procedural requirements. The right candidate will have: +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …dose level selection presentations, on-site CRO monitoring, data and report review , and study archival **Specific Job Responsibilities:** * Coordinates all aspects ... conducting a non-clinical study, with minimal supervision. * Drafts and coordinates review of relevant documents including protocols and study reports. * Coordinates… more
- Translational Research in Oncology (Los Angeles, CA)
- If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is ... clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs),… more
- Cedars-Sinai (CA)
- …or patient contact for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of ... **Job Description** Primary Duties and Responsibilities The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program… more
- Cedars-Sinai (Los Angeles, CA)
- …or patient contact for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of ... required-transportation will be provided for outreach travel. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program… more