- Insmed Incorporated (San Francisco, CA)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional ... strong related experience.Other Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical … more
- BeOne Medicines (Emeryville, CA)
- **General Description:** Reporting to the Head/ Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical ... embed diversity into study design and site selection. The Associate Director will build trusted partnerships with...internal operations under the leadership of the Head of Clinical Trial Diversity + Primary focus is… more
- Merck & Co. (South San Francisco, CA)
- …manufacturing to manage clinical development projectsAssist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead in ... Job DescriptionThe Clinical Director (Principal Scientist) has primary...Immunology, Clinical Investigations, Clinical Medicine, Clinical Research, Clinical Trial Planning,… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The ** Associate Director ** **,** **Digital Clinical Operations** is responsible to enhance Global Clinical Operations' ... Study Startup to Study Close Out with focus on use of Clinical Trial Management System (CTMS) application. This role will specifically focus on following… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The Associate Director , Digital Clinical Operations - Project Lead, is responsible for coordinating and managing digital initiatives ... refinement to ensure digital capabilities meet business needs and regulatory standards. The Associate Director is expected to: + Coordinate and oversee the… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The Advanced Analytics team at BeOne is seeking an Associate Director , Pipeline Analytics to drive data-driven insights into pipeline ... predictive models and scenario analysis frameworks to assess asset progression probability, clinical trial outcomes, and market access feasibility. + Utilize… more
- BeOne Medicines (Emeryville, CA)
- …staffing levels that will enable the delivery of the BeOne clinical trial portfolio. Reporting to the Director of Global Resource Management, this individual ... algorithm development to model future resource demand for various roles within clinical development. The role will also focus on analyzing data and generating… more
- BeOne Medicines (Emeryville, CA)
- …healthcare discipline* with minimum of 8 years of combined experience in Feasibility, Clinical Data Analytics, Clinical Trial Management, and Operations ... analytics and systems, the Global Strategic Feasibility Analytics Lead collaborates with clinical development and clinical operations stakeholders to foster a… more
- BeOne Medicines (Emeryville, CA)
- …Involved in research activities for innovative statistical methods and applications in clinical trial development. ? **Other Qualifications:** + Experiences with ... cross-functional study/project teams supporting hematology studies and interact with Clinical , Regulatory, Statistical Programming, Data Management and other Research… more
- Pfizer (South San Francisco, CA)
- **Job Summary** The Associate Director , Clinical Development Medical Director : + Is accountable for the medical & scientific integrity of the study and ... clinical operations, and other functional lines. The Associate Director , Clinical Development Medical... trials and supports appropriate interpretation and communication of clinical trial data. + Maintains compliance with… more
- Gilead Sciences, Inc. (Foster City, CA)
- …specializes in process improvements, procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director will be a key ... and help create possible, together. **Job Description** **Overview** : The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …associated capabilities to support the CDS objectives + Manage quality review of clinical trial documents, workflows, and outputs within the CDS organization to ... ensure clinical trials are conducted in compliance with Gilead procedures,...+ Analyze new regulations and polices with emphasis Good Clinical Practices (GCP) and partner with business experts and… more
- Pfizer (South San Francisco, CA)
- …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... **JOB SUMMARY** The **A** **ssociate** ** Director , Oncology Biometrics** is a skilled biostatistician who...the reporting of clinical trial results to regulatory authorities and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …timelines. This may include, but is not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical ... Reviewing and analyzing safety reporting, biomarker analyses, and other aspects of clinical trial monitoring. + Using advanced statistical software, methods, and… more
- Bristol Myers Squibb (Brisbane, CA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** ... etc. + Co-lead the cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments in… more
- AbbVie (South San Francisco, CA)
- …this team will have a direct impact on the future success of AbbVie. As Associate Director , Innovation, you will partner with leaders across AbbVie to optimize ... the breadth of drug development (eg product development & manufacturing, trial design, evidence package evaluation, clinical acceleration, commercial… more
- Gilead Sciences, Inc. (Foster City, CA)
- …documents including safety reports, amendments, supplements and license renewals to clinical trial applications and marketing authorizations original INDs/CTAs ... and NDAs/MAAs for assigned territories. + Responsible for preparation of the Company Core Data Sheets (CCDS) for assigned products. + Contributes to the regulatory review of draft Product Company Core Safety Information (CCSI) and ensures updates to the CCDS… more
- Merck (South San Francisco, CA)
- …to manage clinical development projects + Assist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead in ensuring ... **Job Description** The ** Clinical Director (Principal Scientist)** has primary...Immunology, Clinical Investigations, Clinical Medicine, Clinical Research, Clinical Trial Planning,… more
