- IQVIA (Carlsbad, CA)
- …or prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical ... IQVIA is hiring Clinical Research Associates (CRA) at the...visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP)… more
- Abbott (Alameda, CA)
- …in life sciences preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate education and experience. + ... and clinical management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Proficient with Microsoft Suite **What We Offer** At Abbott,… more
- IQVIA (Carlsbad, CA)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Sumitomo Pharma (Sacramento, CA)
- …of medical terminology, and FDA and ICH regulations/guidance documents specific to clinical research and general product development in the pharmaceutical ... a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director… more
- BeOne Medicines (Emeryville, CA)
- …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 with ... ICH-GCP guidelines, local regulations, and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret ... regulatory intelligence specialists have continued access to regulatory , clinical trial, and public domain information...practices. + Review overall quality of ad hoc query research for requested regulatory topics and confirm… more
- BeOne Medicines (Emeryville, CA)
- …and community-based sites to assess, communicate, and enhance representativeness in clinical research . + Contribute to internal presentations, dashboards, and ... + Conduct stakeholder mapping and landscape analyses to monitor evolving clinical research and patient-participation trends **Supervisory Responsibilities:** May… more
- J&J Family of Companies (Irvine, CA)
- …and with internal teams: medical affairs, data management, biostatistics, data programmers, and regulatory affairs + Ensure clinical research studies follow ... Description:** Johnson and Johnson is currently seeking a **Senior Clinical Research Scientist** to support the external... clinical landscapes, and a thorough understanding of clinical trials, regulatory guidelines, and clinical… more
- Stanford University (Stanford, CA)
- …assigns trial workload and manages performance through coaching and supervision of Clinical Research Coordinator Associate , Med. Students, Med scholars, ... Clinical Research Coordinator 2 **School of...with Microsoft Office and database applications. + Experience with research protocols and regulatory or governing bodies,… more
- University of Southern California (Los Angeles, CA)
- …Population and Public Health Sciences invites applications for a full-time Postdoctoral Scholar Research Associate in clinical and translational addiction ... research settings. Experience with the development of regulatory and protocol materials to support clinical ...of regulatory and protocol materials to support clinical research studies (eg, IRB applications, study… more