- Bristol Myers Squibb (San Diego, CA)
- …clinical operations, regulatory, legal, etc + Collaborate with operations to ensure drug shipments, milestones, etc. are aligned to study specific timelines ... for activities associated with activation, tracking, and reporting of study -related information. This role will work cross-functionally with several departments… more
- Sumitomo Pharma (Sacramento, CA)
- …the medical and scientific aspects of clinical trials, including protocol design, study endpoints, and data analysis. + Provide medical expertise to cross-functional ... programs, ensuring that the design, implementation, and conduct of the clinical studies provide unambiguous data and information that allows for clear decision… more
- University of Southern California (San Diego, CA)
- …trials. Incumbent will provide oversight to the progress of clinical trials at study sites, and ensure that they are conducted, recorded, and reported in accordance ... for assigned clinical sites and co-monitor visits. Review Investigator Site Files, study data, perform IP reconciliation, review Informed Consent Forms, and other… more
- BeOne Medicines (Emeryville, CA)
- …and implementation of risk identification and management strategy for clinical studies and other regulated drug development activities. Works collaboratively ... procedures, regulations and tools intended for use in clinical study conduct and other regulated drug development...in clinical study conduct and other regulated drug development activities to ensure compliance with GMP and… more
- Kelly Services (Thousand Oaks, CA)
- …Research Associate with strong in vivo pharmacology expertise to support early-stage drug development. This contract role offers the opportunity to contribute to the ... design and execution of preclinical studies , working closely with multidisciplinary teams in a fast-paced, innovation-driven environment. Job Specifications: Job… more
- IQVIA (Los Angeles, CA)
- …Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies . This is done in a strictly scientific, non-promotional manner, and in ... the initiation and conduct of prioritized Company clinical trials. + Supports clinicals study sites with knowledge and training on the disease, the treatment, the… more
- Cedars-Sinai (Beverly Hills, CA)
- …you will be responsible for the financial management of clinical research studies during the pre-award phase. You will collaborate with principal investigators and ... study teams to develop and negotiate budgets, review contracts,...research finance to support the successful launch of clinical studies . The Clinical Research Budget Coordinator II develops complex… more
- United Therapeutics (Sacramento, CA)
- …advocacy function at various internal cross-functional team meetings + Provide study recruitment support and patient partnership + Enhance patient recruitment for ... research including clinical trials, medical affairs studies , HEOR studies , qualitative research, and human factors studies + Identify opportunities for… more
- University of Southern California (Los Angeles, CA)
- …monitoring visits and responds to inquiries. + Performs follow up for study patient survival by reviewing medical records. Contacts other institutions for data ... in-house, National Cancer Institute (NCI) sponsored and Cooperative Group studies . Discerns basic data discrepancies/protocol violations. Assists in obtaining… more
- Gilead Sciences, Inc. (Foster City, CA)
- …are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available ... Job Requirements:** . Responsible for managing supplies for dynamic clinical studies associated with multiple clinical development programs across the lifecycle of… more