- AbbVie (South San Francisco, CA)
- …remarkable impact on people's lives across several key therapeutic areas - immunology, oncology , neuroscience, and eye care - and products and services in our ... team within CDOR (Clinical Data Operation and Reporting) in OED ( Oncology Early Development) clinical development organization. The stat programming team performs… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and promotional areas, as well as overall industry trends. This role will report into the Global CI Lead for Oncology and will be based in Foster City ... (including Commercial, Medical Affairs, Affiliates, Clinical, Research, Corporate Development, Regulatory , and Legal) as well as Senior Leadership. You...questions that you will define in partnership with the Global CI Lead for Oncology … more
- Pfizer (San Francisco, CA)
- …trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. You may have managerial responsibility for one or more direct ... reports and/or contingent worker(s). You will be the Oncology Clinical Development expert for assigned studies maintaining current scientific and clinical knowledge.… more
- AbbVie (South San Francisco, CA)
- …more clinical development projects through own efforts or those of a team. Lead /develop statistical strategy for project development and regulatory submission. + ... people's lives across several key therapeutic areas - immunology, oncology , neuroscience, and eye care - and products and...of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in… more
- AbbVie (South San Francisco, CA)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as ... remarkable impact on people's lives across several key therapeutic areas - immunology, oncology , neuroscience, and eye care - and products and services in our… more
- Pfizer (South San Francisco, CA)
- …issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities. + Lead and contribute to development and ... position will be responsible for supporting clinical trial(s) and lead subteams in clinical development. The successful candidate should...maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the… more
- Lilly (South San Francisco, CA)
- …leading large clinical trials, preferably in oncology + Ability to lead and work effectively cross-culturally with global colleagues and with TPOs, ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
- Pfizer (South San Francisco, CA)
- …issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities. + Lead and contribute to development and ... including eligibility assessment, data review and safety monitoring. + Lead peer-to-peer interactions with investigator. + Serve as the...maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the… more
- Ascendis Pharma (Palo Alto, CA)
- …Product Management, and Leadership teams to develop and implement the US and global regulatory affairs plan across products + Oversee development and refinement ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...Today, we're advancing programs in Endocrinology Rare Disease and Oncology . The Sr. Director, Regulatory Affairs will… more
- BeOne Medicines (San Mateo, CA)
- …and Patient Affairs, North America and International. This individual will build and lead a new Global Patient Affairs function dedicated to embedding the ... levels of decision-making. + Ensure patient affairs initiatives comply with global , regional, regulatory requirements and ethical standards. **Patient Advocacy… more