Trabajo clinical research associate 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...

A leading biotech company is seeking a Senior Director of Clinical Business Operations to oversee clinical vendor management and ensure successful clinical trials. The candidate will lead RFP processes, negotiate contracts, and establish partnerships with vendors, requiring at least 15 years of experience in clinical research or a related field. This role offers a dynamic environment where...

A leading biotech company is seeking a Senior Director of Clinical Business Operations to oversee clinical vendor management and ensure successful clinical trials. The candidate will lead RFP processes, negotiate contracts, and establish partnerships with vendors, requiring at least 15 years of experience in clinical research or a related field. This role offers a dynamic environment where...

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 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, 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...

A global biotech company in San Francisco is seeking an Associate Director for Regulatory Affairs CMC to develop and execute regulatory strategies. The ideal candidate should have at least 8 years of experience in clinical research or pharmaceuticals and a strong background in global CMC regulatory processes. This role involves collaborating with cross-functional teams, ensuring compliance with...

Role Summary Associate Director, Regulatory Affairs CMC, reporting to the Senior Director, Regulatory Affairs CMC, responsible for developing and executing CMC regulatory strategies for Olema products in development and post-approval. Ensure strategies align with Health Authority requirements globally and provide guidance for high-quality, on-time CMC sections of regulatory submissions, plus...

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 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 Associate Director, Regulatory Affairs will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy. Responsible for leading a comprehensive and strategic approach to developing and executing integrated global regulatory strategies that account for the...

Role Summary The Sr. Manager, Training is an experienced professional with a track record of success in learning and development within the biopharmaceutical industry. The role focuses on developing clinical expertise in assigned disease states and products, managing complex projects, and influencing stakeholders in a fast-paced environment. The candidate should have strong knowledge of rare...

Role Summary The Sr. Manager, Training is an experienced professional with a track record of success in learning and development within the biopharmaceutical industry. The role focuses on developing clinical expertise in assigned disease states and products, managing complex projects, and influencing stakeholders in a fast-paced environment. The candidate should have strong knowledge of rare...

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...

A leading biotech company is seeking a Senior Director of Clinical Business Operations to oversee clinical vendor management and ensure successful clinical trials. The candidate will lead RFP processes, negotiate contracts, and establish partnerships with vendors, requiring at least 15 years of experience in clinical research or a related field. This role offers a dynamic environment where...

A global biotech company in San Francisco is seeking an Associate Director for Regulatory Affairs CMC to develop and execute regulatory strategies. The ideal candidate should have at least 8 years of experience in clinical research or pharmaceuticals and a strong background in global CMC regulatory processes. This role involves collaborating with cross-functional teams, ensuring compliance with...

Role Summary Associate Director, Regulatory Affairs CMC, reporting to the Senior Director, Regulatory Affairs CMC, responsible for developing and executing CMC regulatory strategies for Olema products in development and post-approval. Ensure strategies align with Health Authority requirements globally and provide guidance for high-quality, on-time CMC sections of regulatory submissions, plus...

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 As the Director, Medical Affairs, reporting into the Sr Director, Skeletal Dysplasia, you will help shape the future of care for individuals with skeletal dysplasias by developing and executing the medical strategy behind infigratinib’s development and launch. You will serve as the scientific voice connecting clinicians, researchers, advocacy groups, and internal teams, ensuring our...

Role Summary Director for the Aesthetics & Regenerative Medicine HEOR-Strategy team to lead strategic research for pipeline and on-market products, supporting approval, reimbursement, and differentiation. The role requires expertise in patient-centered outcomes research, HEOR strategy, and regulatory submissions, with responsibilities spanning both cash-pay and reimbursed portfolios. The Director...