- BeOne Medicines (San Mateo, CA)
- **General Description:** The Director, Global Clinical Operations, Compliance builds, collaborates and manages key relations to better support and understand the ... of the business and drive the compliance activities within Global Clinical Operations. Provides quality guidance, direction...regulatory environment, ICH GCP, applicable laws, regulations, and industry standards as it relates to a global … more
- GRAIL (Menlo Park, CA)
- …and healthcare companies. For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead data management activities ... closely with GRAIL study team members to ensure that clinical data captured is complete, consistent, and...Management and other GRAIL staff with developing and implementing data standards , controlled procedural documents, and software… more
- BeOne Medicines (San Carlos, CA)
- …advisor to BeOne's Global Research & Development (R&D) functions, including Global Clinical Operations, Clinical Development, and other Research ... in the biopharmaceutical or life sciences industry. + Strong understanding of global clinical development, research operations, and global regulatory… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The Director, Global Regulatory Project Management (Director, Global RPM) is a senior strategic leader responsible for supporting, ... influencing, translating, and executing oncology regulatory strategies across the global drug development lifecycle. This role combines deep regulatory expertise… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The Associate Director, Global Regulatory Project Management (AD, Global RPM) is a strategic leader responsible for translating and ... executing regulatory strategies across the global drug development lifecycle. This role blends deep regulatory expertise with advanced project management skills,… more
- Parexel (Sacramento, CA)
- …+ When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical ... in a CRO or pharma organization + Preferred therapeutic experience in Oncology + Global clinical trial experience preferred + Extensive knowledge of clinical … more
- BeOne Medicines (Emeryville, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... Word, Excel, PowerPoint and Outlook - Familiar with industry CTMS and data management systems **Other Qualifications:** - Understands clinical trial processes… more
- GRAIL (Menlo Park, CA)
- …controls and data -delivery mechanisms that uphold stringent blinding and privacy standards . + Partner with Research, Clinical Lab Operations, and Software ... through analysis, ensuring every step meets rigorous regulatory and clinical standards . We are seeking a Staff...you will collaborate with cross-functional teams to deliver scalable data solutions aligned with FDA and global … more
- BeOne Medicines (San Mateo, CA)
- **General Description:** Join BeOne's Global Data Strategy and Solutions team to build and scale a cutting-edge and fully integrated Enterprise Data and ... etc.) through quick hands-on evaluations. + Develop and enforce data governance standards , including data ...technologies and frameworks. + Experience working with Life Sciences data , including exposure to R&D, Clinical Operations,… more
- Parexel (Sacramento, CA)
- …The Manager, Central Monitoring is accountable for centralized monitoring activities for global and/or complex trials, analytical data review of key risk ... a focus on interpreting KRIs and KPIs + Knowledge and experience with clinical databases, electronic data capture systems, quality control processes, and… more
