Trabajo clinical data en Estado de Oaxaca

Role Summary Senior Director of Clinical Business Operations, reporting to the SVP of Clinical Operations. Supports the Clinical Department’s initiatives to contribute to the success of clinical trials, develops global outsourcing strategy, and partners with clinical study teams to organize vendor selection, RFP processes, bid defenses, and contract negotiations. Based in San Francisco or...

Role Summary Senior Director of Clinical Business Operations, reporting to the SVP of Clinical Operations. Supports the Clinical Department’s initiatives to contribute to the success of clinical trials, develops global outsourcing strategy, and partners with clinical study teams to organize vendor selection, RFP processes, bid defenses, and contract negotiations. Based in San Francisco or...

Role SummarySenior Director of Clinical Business Operations, reporting to the SVP of Clinical Operations. Supports the Clinical Department's initiatives to contribute to the success of clinical trials, develops global outsourcing strategy, and partners with clinical study teams to organize vendor selection, RFP processes, bid defenses, and contract negotiations. Based in San Francisco or...

Role Summary The Sr. Manager, Clinical Supply Chain Management & Operational Excellence leads continuous improvement efforts to streamline SOPs and enhance efficiency across the end-to-end clinical supply chain. This role coordinates IMP planning, forecasting, labeling, packaging, distribution, inventory monitoring, and reconciliation for assigned clinical studies, and collaborates with QA,...

Role Summary The Head of Oncology Solid Tumors Medical Affairs is responsible for leading and overseeing the global medical affairs strategy, execution, and scientific leadership for the oncology solid tumor portfolio. This role requires expertise in oncology drug development, clinical trials, regulatory interactions, and cross-functional collaboration. The Head will serve as the key medical...

Role Summary Senior Director of Biostatistics, reporting to the VP of Biostatistics, you will lead the statistical strategy and execution of a pivotal Phase 3 clinical trial and all associated NDA activities. You will apply and share knowledge of appropriate statistical methods for clinical trial design and data analysis, and collaborate cross-functionally to support planning, execution, and...

Role Summary Executive Director, Medical Writing responsible for establishing and managing the Cardiorenal Medical Writing group within BridgeBio, overseeing development and finalization of clinical and regulatory documents, and guiding internal and external Medical Writers to deliver high-quality submissions and disclosures in regulatory programs. Responsibilities Oversee the Cardiorenal Medical...

Role Summary Senior Statistical Programmer reporting to the Principal Statistical Programmer, accountable for all assigned statistical programming deliverables in adherence to company SOPs and ICH/GCP. Opportunity to work on late phase trials and contribute to patient care in breast cancer. Based in San Francisco with approximately 10% travel. Responsibilities Conduct hands-on validation/QC of...

Role Summary The Associate Director, Marketing & Sales will support project management and commercialization of key assets. The Associate Director, Marketing & Sales will drive cross-functional collaboration and tactical alignment, ensuring success in the US and will serve as a pivotal point to support the critical functions of marketing and sales to optimize collaboration. This individual will...

Role Summary The Director of Trade Compliance and Logistics will oversee global logistics operations and international trade compliance across the organization’s supply chain. This leadership role develops and implements effective logistics strategies that support the product supply chain while ensuring adherence to global trade regulations. The position leads logistics team members, manages...

Role Summary The Associate Director, GLP/GCP Quality Audits and Compliance plays a critical role in protecting data integrity and regulatory readiness across the company’s nonclinical and clinical portfolio. This position leads the planning, execution, and reporting of internal and external GLP/GCP audits, ensuring compliance with U.S. and international regulations while driving continuous...

Role Summary The Director, Marketing – Patient & HCP will lead the development and commercialization of key assets, with primary responsibility for driving integrated patient and healthcare provider (HCP) marketing strategy in the US. This role will provide strategic leadership across patient- and HCP-facing initiatives for the launch and growth of BBP-418 and future assets. The Director will...

Role Summary Senior Director of Biostatistics, reporting to the VP of Biostatistics, you will lead the statistical strategy and execution of a pivotal Phase 3 clinical trial and all associated NDA activities. You will apply and share knowledge of appropriate statistical methods for clinical trial design and data analysis, and collaborate cross-functionally to support planning, execution, and...

Role Summary The Director of Trade Compliance and Logistics will oversee global logistics operations and international trade compliance across the organization’s supply chain. This leadership role develops and implements effective logistics strategies that support the product supply chain while ensuring adherence to global trade regulations. The position leads logistics team members, manages...

Role Summary The Associate Director, Marketing & Sales will support project management and commercialization of key assets. The Associate Director, Marketing & Sales will drive cross-functional collaboration and tactical alignment, ensuring success in the US and will serve as a pivotal point to support the critical functions of marketing and sales to optimize collaboration. This individual will...

Role Summary The Associate Director, GLP/GCP Quality Audits and Compliance plays a critical role in protecting data integrity and regulatory readiness across the company’s nonclinical and clinical portfolio. This position leads the planning, execution, and reporting of internal and external GLP/GCP audits, ensuring compliance with U.S. and international regulations while driving continuous...

Role Summary Executive Director, Medical Writing responsible for establishing and managing the Cardiorenal Medical Writing group within BridgeBio, overseeing development and finalization of clinical and regulatory documents, and guiding internal and external Medical Writers to deliver high-quality submissions and disclosures in regulatory programs. Responsibilities - Oversee the Cardiorenal...

Role Summary The Head of Oncology Solid Tumors Medical Affairs is responsible for leading and overseeing the global medical affairs strategy, execution, and scientific leadership for the oncology solid tumor portfolio. This role requires expertise in oncology drug development, clinical trials, regulatory interactions, and cross-functional collaboration. The Head will serve as the key medical...

Role Summary The Director, Marketing – Patient & HCP will lead the development and commercialization of key assets, with primary responsibility for driving integrated patient and healthcare provider (HCP) marketing strategy in the US. This role will provide strategic leadership across patient- and HCP-facing initiatives for the launch and growth of BBP-418 and future assets. The Director will...

Role Summary Senior Statistical Programmer reporting to the Principal Statistical Programmer, accountable for all assigned statistical programming deliverables in adherence to company SOPs and ICH/GCP. Opportunity to work on late phase trials and contribute to patient care in breast cancer. Based in San Francisco with approximately 10% travel. Responsibilities - Conduct hands-on validation/QC...