- Gilead Sciences, Inc. (Foster City, CA)
- …limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample size, authoring ... team members and cross-functional partners. Provides statistical consultation on trial design and study endpoints and authors statistical analysis plans.… more
- Cedars-Sinai (Los Angeles, CA)
- …coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent ... including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the… more
- Robert Half Legal (Los Angeles, CA)
- …templates and incorporating information provided by attorneys and adjusters. * Organize trial preparation materials, including exhibits, witness lists, and trial ... tasks, including drafting requests and responses. * Strong knowledge of trial preparation processes and legal pleadings. * Familiarity with electronic filing… more
- Cedars-Sinai (CA)
- …including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent ... including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the… more
- Cedars-Sinai (Los Angeles, CA)
- …including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent ... including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the… more
- Gilead Sciences, Inc. (Foster City, CA)
- …**Job Responsibilities** + Lead the development and execution of clinical trial protocols for inflammation programs, ensuring scientific rigor and regulatory ... throughout the clinical development lifecycle. + Analyze and interpret clinical trial data; contribute to clinical study reports, regulatory submissions, and… more
- BeOne Medicines (San Mateo, CA)
- …that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in ... country teams to ensure that country and site level Trial Master File is created, maintained and QC'd on...in study for countries in region + Manages the trial data collection process for the region, drives data… more
- Edwards Lifesciences (Irvine, CA)
- …complex clinical study contracts with third-party vendors to support clinical trial operations. In alignment with applicable regulations and Edwards Lifesciences ... on full knowledge of financial, regulatory and clinical requirements + Negotiate trial budgets with clinical sites to ensure compliance with company- approved… more
- Astrix Technology (El Segundo, CA)
- …**Location:** Remote **Responsibilities:** + Oversee and regularly update the Clinical Trial Quality Management system to ensure alignment with current industry ... (CAPAs). + Organize, coordinate, and execute audits of vendors, suppliers, clinical trial sites, as well as internal and compliance audits, including for-cause… more
- Drug Enforcement Administration (San Diego, CA)
- …may be required to serve a 1-year probationary period or 1 or 2-year trial period during which we will evaluate your fitness and whether your continued employment ... of the Federal service. Upon completion of your probationary period or trial period your employment will be terminated unless you receive certification, in… more