- Gilead Sciences, Inc. (Foster City, CA)
- …together. **Job Description** You may act as a Clinical Development Lead and Physician Responsible on clinical trial programs in the Inflammation and ... lifecycle management of the assigned products + Leads or otherwise oversees and directs clinical trial protocol design and clinical study reporting for… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of these tasks if outsourced. You will provide safety science input into clinical trial protocols, develop appropriate regulatory responses, and provide the ... from third parties, such as regulatory agencies. + Performs safety reviews of clinical trial protocols, Investigator's Brochures, clinical study reports,… more
- Bristol Myers Squibb (Brisbane, CA)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... various departmental initiatives (eg, committees, sub-teams etc.) + Presents and/or articulates clinical strategy to senior leadership and to support progression… more
- Pfizer (San Francisco, CA)
- …alignment with the Lifecycle Management Plan and Integrated Product Plan * Endorses clinical decisions in advance of GPT, senior management reviews or governance ... management responsibilities of medical director(s) * Accountable for the clinical development strategy, trial design, execution, and...the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …third parties, such as regulatory agencies. + May perform safety reviews of clinical trial protocols, Investigator's Brochures, clinical study reports, ... an experienced Global Therapeutic Area (TA) Safety Scientist or Physician . **Key Responsibilities will include, but are not limited...college + Must be a Rising Sophomore, Junior, or Senior in undergrad or a Graduate or Doctoral Student… more