- Gilead Sciences, Inc. (Foster City, CA)
- …with chronic liver diseases including various cholangiopathies. + Experience in the biopharma industry is strongly preferred . + Multiple years' experience ... may include, but are not limited to, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …disease training (eg Rheumatology, Allergy/Immunology, or Dermatology) + Experience in the biopharma industry is preferred but not required. + Experience leading ... are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with IBD management or inflammatory disease management.. + Experience in the biopharma industry is preferred . + Significant experience working on, with ... are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …applicants with experience in hepatitis D and/or B. + Relevant experience in Hepatology is preferred . + Experience in the biopharma industry is preferred . + ... clinical development component(s) in the preparation/review of regulatory documents, investigator brochures and development plans. + Coordinates the collection and… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …years of clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia ** Preferred Qualifications** + Board ... to design and implement clinical studies + Write protocols, investigator brochures, clinical study reports and review clinical trial...of the Rehabilitation Act of 1973, the Vietnam Era Veterans ' Readjustment Act of 1974, and Title I of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …or related experience supporting medicinal products. + Significant experience in the biopharma industry is strongly preferred . + Experience authoring a broad ... complexities, such as clinical study reports (CSRs all phases, investigator 's brochures, CTD summaries/overviews, PIPs/PIP modifications, and regulatory responses).… more
- Catalent Pharma Solutions (Bloomington, IN)
- …appropriate corrective and/or preventive actions (CAPA) to prevent reoccurrence. The Investigator assists Operations and Quality Assurance teams to determine the ... + Bachelor's degree in a STEM discipline. + Master's degree or higher preferred . + 5-8 years of pharmaceutical manufacturing experience, or related. + 2 years… more