- Amgen (South San Francisco, CA)
- …change the world. In this vital role you be a part of Amgen's Clinical Pharmacology, Modeling and Simulation (CPMS) department focusing on use of data science and ... the pharmacometric modeling to make robust inferences to support clinical drug development across diverse therapeutic areas. **Responsibilities:** + Designs… more
- Envista Holdings Corporation (Pomona, CA)
- …gaps related to material compatibility and propose robust solutions or independent studies . + Design and carry out developmental work using appropriate methods and ... to facilitate formula development process. + Perform material compatibility study for surface disinfectant wipes and liquids as per...compatibility testing. + Collaborate and carry out design verification studies and other studies to meet the… more
- IQVIA (Sacramento, CA)
- …trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, ... bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role… more
- Sumitomo Pharma (Sacramento, CA)
- …relationships with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
- Parexel (Sacramento, CA)
- …in leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or Real World Data, with a good understanding of molecule and ... West Coast hours. **About Us:** At Parexel, we are dedicated to advancing clinical research and supporting medical affairs with innovative solutions. We are seeking… more
- Parexel (Sacramento, CA)
- …Partner is a crucial liaison for investigative sites throughout a study 's lifecycle, responsible for site start-up, activation, relationship management, recruitment, ... + Maintains a knowledge of assigned protocols + Conducts study start-up activities at the site level including but...for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness… more
- AbbVie (South San Francisco, CA)
- …Statistical Programming and other stakeholders to evaluate existing databases, both clinical studies and real-world databases, assist with feasibility assessment ... our patients. Responsibilities: + Contribute to design, analysis and reporting of clinical trials or other scientific research studies . Assist with development… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …maintain the effectiveness of the Otsuka Quality Systems that support OPDC-sponsored clinical studies as well as drive continuous improvement. **Job ... and escalation of any situations with potential negative impacts on clinical study supplies, supply chain for commercial products, or patient safety.… more
- The County of Los Angeles (Los Angeles, CA)
- …in nearly every medical specialty and subspecialty. In addition, to its direct clinical services, DHS also runs the Emergency Medical Services (EMS) Agency and the ... microtome or ultramicrotome instruments, paraffin and plastic sections for study and viewing by a pathologist using light and...surgical specimens to be processed for routine or special studies by light and/or electron microscopy. + Prepares and… more
- InGenesis (Sunnyvale, CA)
- …role, you will be responsible for conducting audiological procedures in the context of user studies . The current study duration is 10 - 12 months. If you meet ... Job Duties * Conduct audiological procedures in the context of user studies . * Audiological procedures may include otoscopy, tympanometry, audiometry, and ear… more