- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …report (FSR), including authoring statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
- System One (Walnut Creek, CA)
- … research trials at various US based sites. The SI performs delegated clinical and research duties, ensuring compliance with study protocols, ethical standards, ... direct supervision of the PI. Key Responsibilities + Conduct clinical assessments and patient study visits. + Assist the PI in participant screening, eligibility… more
- University of Southern California (Los Angeles, CA)
- …organized individual who is able to effectively communicate with participants, clinical and research staff, and program investigators. The Research Coordinator II ... + Interacting with other departments and core resources at NCCC ( Clinical staff, Data Sciences Core, Translational Pathology Core, etc) to identify… more
- Veterans Affairs, Veterans Health Administration (San Diego, CA)
- …of the requirements below: (1) Successful completion of a full four-year course of study from an accredited college or university, leading to a bachelor's or higher ... degree, that included a major study in an academic field related to health sciences...a histopathology technologist, such as, but not limited to clinical biology, microbiology, physiology, pre-medical, medical lab technology, chemistry,… more
- Cytel (Sacramento, CA)
- The Senior Medical Coder plays a critical role in supporting clinical trials by ensuring the accurate, consistent, and timely coding of medical terms using ... WHO Drug). This individual brings advanced knowledge of medical terminology, clinical trial processes, regulatory requirements, and coding best practices. The Senior… more
- Parexel (Sacramento, CA)
- …practice + Interact with clients and regulatory authorities + Review publications and clinical study reports + Travel to, attend, and actively contribute to ... work remotely. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will… more
- IQVIA (San Francisco, CA)
- …with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work ... line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with… more
- ManpowerGroup (Sunnyvale, CA)
- Our client, a leading organization in clinical research and healthcare services, is seeking a dedicated Phlebotomist III to join their team. As a Phlebotomist III, ... essential part of the research support staff, contributing to vital scientific studies and patient care. The ideal candidate will demonstrate strong initiative,… more
- University of Southern California (Los Angeles, CA)
- …case reviews for all potential encounters generated from transplant patients and time studies for both staff and physicians/surgeons. The TCS is responsible for the ... review. Responsible for resolving any questionable charges, activities with the clinical staff and managers. + 2. Reviews and directs appropriate pre-transplant… 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