- Gilead Sciences, Inc. (Foster City, CA)
- …products that are benefiting millions of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available ... and improve life by advancing the care of patients with life-threatening diseases. Director , Compensation Design - Fair Pay/Pay Equity **Job Summary** : We are… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening ... and serious respiratory and cardiovascular conditions. **KEY RESPONSIBILITIES** The Director , CMC Regulatory Affairs for Biologics is responsible for defining… more
- Gilead Sciences, Inc. (Foster City, CA)
- …products that are benefiting millions of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available ... engagement?". As a member of our world-class People Analytics team, the Associate Director , Insight Partner has the opportunity to convert global data into answers… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** As Sr. Director of Clinical development in the Inflammation/Fibrosis therapeutic area, you will ... Qualifications:** + MD or equivalent with 6+ years clinical, scientific, and/or drug development experience in the biopharma industry, academia, or a related… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Examples include meeting requests, briefing packages, original Investigational New Drug (IND), IND amendment, and routine submissions (eg, Development Safety ... and teams with responsibilities related to clinical trials or other drug development activities. + Experience and proven effectiveness working and negotiating… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Examples include meeting requests, briefing packages, original Investigational New Drug (IND), IND amendment, and routine submissions (eg, Development Safety ... projects and teams with responsibilities related to clinical trials or other drug development activities. + Line management (direct reports) experience is preferred.… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with 12+ years' relevant experience. + 6+ years' experience in prescription drug labeling. + Significant experience leading development of regulatory labeling or ... of successes working and negotiating with regulatory authorities. + Global prescription drug label experience, US, EU, and potentially more. + Extensive experience… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with 10+ years' relevant experience. + 4+ years' experience in prescription drug labeling. + Significant regulatory experience in the biopharma industry is strongly ... with one or more Gilead therapeutic areas and varying stages of drug development is strongly preferred. **Knowledge & Other Requirements** + In-depth knowledge… more
- Gilead Sciences, Inc. (Foster City, CA)
- …but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance. + Manages the clinical development component(s) in the ... Experience** + MD or equivalent with 4+ years' clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or… more
- Gilead Sciences, Inc. (La Verne, CA)
- …in North America, including Customer Service, US logistics and commercial drug product shipments.Managing all aspects of warehousing and transport including Safety, ... to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974,… more