- Sumitomo Pharma (Sacramento, CA)
- … studies , supporting statistical design, authoring statistical sections of study protocols and Statistical Analysis Plans (SAPs), and supporting trial design, ... of Manager of Biostatistics to serve as trial statistician for one or more clinical studies . He or she works closely with the clinical team on the statistical design… more
- Otsuka America Pharmaceutical Inc. (Palo Alto, CA)
- …the responsibilities of supporting the design, conduct, and analysis of preclinical studies for the current and next generation technologies. The position requires a ... and Duties:** * Responsible for supporting the design and conduct of preclinical studies in large animal models to support next generation technologies through close… more
- Cedars-Sinai (Beverly Hills, CA)
- …responsible for all activities associated with clinical study coordination, subject Screening/recruitment/enrollment, data management/integrity, regulatory ... and family members. Coordinates the clinical logistics of the study , and works in tandem with the Research and/or...Diploma in Nursing required. + Minimum 2 years of paid clinical nursing experience in a hospital or clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of assigned clinical trial(s) and oversees clinical trial conduct including study start-up, enrollment, maintenance and close-out. + Prepares and/or contributes to ... development of study -related documents (eg, Clinical protocols, Informed consent forms, Pharmacy...stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include… more
- Parexel (Glendale, CA)
- …do after training is completed (including but not limited):** + You will understand study protocols and be able to complete required medical procedures + Recruit ... study participants by calling the database, attending company sponsored...eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance,… more
- Bristol Myers Squibb (San Diego, CA)
- …to review critical study documents and perform data reviews for ongoing studies + Oversee CDISC data package development for clinical studies to support ... Programming at RayzeBio will be accountable for development of clinical study related deliverables and timelines, oversee study vendors' programming… 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...remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole… more
- Kelly Services (Thousand Oaks, CA)
- …opportunity to contribute to the design and execution of preclinical studies , working closely with multidisciplinary teams in a fast-paced, innovation-driven ... Shift Pay Rate: $40-50/hr Roles and Responsibilities: Conduct in vivo pharmacology studies in rodent models for neurological and cardiovascular indications. Support … more
- Bristol Myers Squibb (San Diego, CA)
- …for activities associated with activation, tracking, and reporting of study -related information. This role will work cross-functionally with several departments ... Affairs IITs, including fair market value assessments for all study related items. Create process for internal review of...processes + Ensure that processes allow for activation of studies in a timely fashion consistent with the developed… 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