- Cedars-Sinai (Los Angeles, CA)
- …all applicable regulatory requirements. + Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including ... our team and contribute to groundbreaking research.** We are seeking a dedicated Clinical Research Coordinator II to join our team. The ideal candidate will have… more
- Lilly (San Diego, CA)
- …on Medical Education (LCME). **Preferred Qualifications** + Minimum 3-5 years of pharmaceutical industry experience in clinical development + PhD in Immunology, ... health authority meeting experience + Advanced degree or fellowship training in clinical research or pharmaceutical medicine + Experience with innovative,… more
- Gilead Sciences, Inc. (CA)
- …and help create possible, together. **Job Description** The Associate Director, Clinical Records & Information Management is responsible for partnering with ... cross-functional teams, Clinical Research Organizations (CROs), and Functional Service Providers (FSPs)...to enhance operational excellence and inspection readiness + Analyze data and audit outputs to identify trends and develop… more
- Cedars-Sinai (Santa Monica, CA)
- …all applicable regulatory requirements. + Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including ... patients with cancer. **Join our team and contribute to groundbreaking research.** The Clinical Research Coordinator II serves as the lead coordinator on an assigned… more
- Abbott (Alameda, CA)
- …and audit Trial Master File to ensure inspection readiness. + Perform review of clinical data listings for completeness and accuracy, and escalate issues to the ... experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Demonstrated excellence in a fast-paced environment, effectively managing multiple clinical project deliverables and priorities through matrix management ... or oversight in the preparation, review, and interpretation of clinical study data , ensuring high quality ...for one or more projects + Thorough understanding of pharmaceutical regulatory requirements and impact on development and execution… more
- BeOne Medicines (Emeryville, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... Word, Excel, PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes… more
- BeOne Medicines (San Carlos, CA)
- **_General Description:_** We are seeking an accomplished Director of Clinical Biomarker & Translational Medicine for Oncology (Solid Tumor Portfolio) to provide ... strategic, scientific, and operational leadership across our clinical biomarker initiatives for solid tumor oncology programs. This role is pivotal in driving the… more
- AbbVie (Irvine, CA)
- …tears, gels and ointments). Leads the direction, planning, and interpretation of clinical trials or research activities within consumer eye care innovation of one ... may lead cross-functional teams to generate, deliver, and disseminate high-quality data supporting consumer eye care product scientific and business strategy.… more
- BeOne Medicines (San Mateo, CA)
- … questions from sites, IRBs/IECs, Health Authorities, and CRO's + Review, query, and analyze clinical trial data . + Interpret, and present clinical trial ... data both internally and externally. + Represent a clinical study or development program on one or more...5 plus years of experience and success within other biotech/ pharmaceutical companies. + Previous participation in a clinical… more