- BeOne Medicines (San Mateo, 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
- 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
- Ascendis Pharma (Palo Alto, CA)
- …+ Provide leadership to study teams + Ensure successful completion of trial -related documents (including clinical trial protocols, investigator brochures, ... Those with less experience may be considered for an Associate Medical Director position. + At least...position. + At least 3 years of experience with clinical trial design and execution + Strong… 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
- BeOne Medicines (San Mateo, 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
- Ascendis Pharma (Palo Alto, CA)
- …dynamic workplace for employees to grow and develop their skills. The Associate Director , Medical Affairs Statistical Sciences Biometrics provides technical and ... the global market access and health economic teams. The Associate Director ensures will be working on...design, data analysis, data mining, epidemiology-related analyses, use of clinical trial data to inform reimbursement strategy… more
- AbbVie (South San Francisco, CA)
- …must be local to San Francisco, CA or Lake County, IL. The Associate Director of Exploratory Statistics provides statistical leadership in drug discovery ... and patient selection or stratification to advance precision medicine. The associate director role collaborates with discovery researchers, translational… more
- Ascendis Pharma (Palo Alto, CA)
- …a dynamic workplace for employees to grow and develop their skills. The Associate Director , Global Medical Writing, will be responsible for writing scientific ... aligned with strategic goals. + Participate in meetings with clinical trial investigators and key opinion leaders...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… 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
- BeOne Medicines (San Mateo, 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
- 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
- BeOne Medicines (San Mateo, 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 (San Mateo, 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
- 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