- Stanford University (Stanford, CA)
- …_* - Other duties may also be assigned._ **DESIRED QUALIFICATIONS:** + Oncology clinical trial coordination experience. Minimum of 2 years experience in a ... clinical research setting. + Investigator Initiated clinical trial coordination experience. **EDUCATION & EXPERIENCE (REQUIRED):** Bachelor's degree in a… more
- University of Southern California (Los Angeles, CA)
- …studies and interprets finished results. + Contributes to the implementation of specific clinical trial protocols and the clinical management of patients ... trials. + Collaborates with other providers to identify potential clinical trial candidates and obtain informed consent when appropriate + Performs all… more
- Bristol Myers Squibb (San Diego, CA)
- …protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct investigator meetings and ... lead site qualification and initiation visits with clinical trial investigators + Execute and deploy drug development strategic plans, develop contingency plans,… more
- Stanford Health Care (Palo Alto, CA)
- …with oncology treatment plans and investigational drug studies. * Ability to interpret clinical trial protocols and translate them into Epic EMR build ... You will directly impact patient safety and the efficiency of oncology clinical trials by building precise IDS (Investigational Drug Study) chemotherapy protocols in… more
- Abbott (Alameda, CA)
- …scientists. **The Opportunity** The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical ... reports, and track resolution of action items. + Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of patients worldwide. **Job Description** You will typically lead multiple components of clinical trial programs in immunology clinical development. You may ... For the assigned projects, you are accountable for various aspects of ongoing clinical trial program-related activities. These activities include, but are not… more
- Gilead Sciences, Inc. (Foster City, CA)
- …diseases. **Job Responsibilities** + Lead the development and execution of clinical trial protocols for inflammation programs, ensuring scientific rigor ... throughout the clinical development lifecycle. + Analyze and interpret clinical trial data; contribute to clinical study reports, regulatory submissions,… more
- Abbott (Pleasanton, CA)
- …knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research ... + As needed, provide clinical and technical expertise for clinical trial procedure support + Attend study procedures and follow-ups (or ensure trained… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …+ Write protocols, investigator brochures, clinical study reports and review clinical trial documents + Conduct investigator meetings and lead site ... initiation visits with clinical trial investigators + Implement and deploy drug development strategic plans, develop contingency plans, provide technical and… more
- Abbott (Pleasanton, CA)
- …knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research ... + As needed, provide clinical and technical expertise for clinical trial procedure support + Attend study procedures and follow-ups (or ensure trained… more