- The County of Los Angeles (Los Angeles, CA)
- …be assigned to the ongoing management of chronic disease patients,subject to periodic review of medical staff. Supervises or performs the preparation of drug labels ... protected from deterioration. Selects, compounds, and dispenses drugs and other pharmaceutical products ordered by physicians, dentists, and other licensed medical… more
- Dignity Health (Bakersfield, CA)
- …operations. Responsible for assuring that all the activities for the provision of pharmaceutical care at their campus are carried out in full accordance with all ... committees. The coordinator is an active participant in the quarterly business review to integrate drug procurement and drug utilization. The coordinator will "take… more
- AbbVie (Irvine, CA)
- …Oversee global clinical study teams monitoring overall study integrity and review , interpretation, and communication of accumulating data pertaining to botulinum ... supervision. + At least 5 years of clinical study experience in the pharmaceutical industry, academia, or equivalent. + Ability to oversee a complex clinical… more
- Cardinal Health (Sacramento, CA)
- Cardinal Health Sonexus (TM) Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford and ... other status protected by federal, state or local law._ _To read and review this privacy notice click_ here… more
- The County of Los Angeles (Los Angeles, CA)
- …and immunizations, and observing clinical symptoms. Monitors inventory levels of pharmaceutical supplies and equipment and assists in inventory maintenance for ... the guides will help you preparing for the test, we advise you to review all related materials that you deem necessary. + An interactive, Online Test Preparation… more
- Mentor Technical Group (South San Francisco, CA)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... system. 2. Maintain client's CMMS updated with any applicable data and/or statuses. 3. Review all work requests submitted to his area assigned group and filter all… more
- Kelly Services (Pleasanton, CA)
- …to ensure alignment with business processes and procedures. + Author and review SOPs and Statistical Analysis Plans (SAPs). + Conduct and report inspections ... preferred. + 10+ years of relevant industry experience in bioanalytical or pharmaceutical company. + Subject matter expert in GLP compliance, regulations, and… more
- Nestle (Los Angeles, CA)
- …Peptamen(R), Compleat Organic Blends(R), and more. We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent, manage, and ... operator: ###. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at https://www.nestlejobs.com/privacy. Job… more
- AbbVie (Irvine, CA)
- …As a clinical development subject matter expert, author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: ... + At least 5 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + Knowledge of clinical trial methodology, regulatory… more
- BeOne Medicines (San Mateo, CA)
- …input related to key deliverables (eg impact to submission timelines). + Review and contribute to the implementation of standards, templates, and procedures related ... + A minimum of 5+ years in the biotechnology or pharmaceutical industry required. + Regulatory operations experience within a regulated environment… more