Clinical Trial Manager Jobs in South San Francisco, CA

Oversee preclinical operations by managing non-GLP and GLP toxicology studies, ensuring scientific and corporate goals are achieved while complying with regulatory standards and fostering collaboratio...

Drive clinical research excellence by managing projects, ensuring compliance, and leading cross-functional teams to deliver high-quality study operations that meet sponsor expectations and regulatory...

Lead the execution of client implementation projects, ensuring alignment across cross-functional teams to enhance operational efficiency and exceed client expectations while driving process improvemen...

Join a team that's shaping the future of oncology project management by overseeing interdisciplinary clinical research studies and ensuring regulatory compliance while enhancing client relationships a...

Elevate the clinical adjudication process by leading cross-functional teams to ensure timely, high-quality project delivery while optimizing workflows and achieving strategic milestones in the pharmac...

Join a team that's driving project success in healthcare by leading clinical adjudication initiatives, enhancing workflows, and collaborating across departments to ensure quality and efficiency in pro...

Lead the charge in advancing clinical research through expert data management and programming. You'll collaborate with a multidisciplinary team to design robust systems, ensuring data integrity and qu...

Drive new business pursuits in the pharmaceutical services sector, fostering strategic partnerships and achieving growth objectives through proactive development and client engagement...

Partner with us to deliver exceptional client service in a dynamic role, guiding pharmaceutical companies and research organizations through IRB processes to ensure timely communication and compliance...

Champion the IRB meeting workflow, ensuring compliance and communication across teams while managing submissions and consent form preparation to uphold human subject protections and regulatory standar...

Transform clinical development through strategic leadership and operational excellence. Drive execution of programs across phases while mitigating risks, ensuring timelines, and leading cross-function...

Lead the charge in delivering global clinical studies from start-up to close-out, ensuring strategic alignment, operational excellence, and stakeholder collaboration. Drive performance, quality, and b...

Lead the charge in managing global clinical studies in orthopedic devices, ensuring adherence to regulations and timelines. Collaborate with diverse teams and drive projects from inception to completi...

Drive advancements in clinical trial technology as a key liaison between Clinical Development and IT, focusing on analysis, implementation, and optimization to enhance global research operations for i...

Drive quality assurance in GMP operations, ensuring compliance and product integrity while collaborating with internal and external stakeholders. Contribute to clinical manufacturing excellence throug...

Champion quality assurance in GMP clinical manufacturing, ensuring compliance and product integrity across drug development and release processes while liaising with internal and external stakeholders...

Accelerate progress at improving Veterans’ health outcomes by leading innovative healthcare pilot projects. Collaborate with senior stakeholders and navigate federal policy to deliver impactful care d...

Architect comprehensive drug development strategies to drive oncology programs, manage cross-functional teams, and ensure project deliverables align with business objectives, fostering innovation and...

Advance your career as a Clinical Supervisor by guiding a dedicated team in delivering exceptional patient care and ensuring compliance with best practices in home health...

Lead the charge in enhancing patient care as a Clinical Supervisor, guiding a dedicated team of nurses and caregivers. Ensure quality, compliance, and effective communication while fostering a support...

Join a dynamic team to oversee clinical study sites, ensuring compliance with regulations and quality standards while fostering strong site relationships and optimizing trial performance across multip...

Oversee and manage large-scale, multi-national projects, ensuring successful delivery through direct team leadership and cross-functional collaboration, while maintaining high quality and financial pe...

Join a team that's at the forefront of medical device evaluation. Leverage your expertise in regulatory affairs and clinical evaluations to guide our medical writers and optimize safety and performanc...

Lead the charge in advancing medical device regulatory projects. Manage clinical evaluation reports, ensuring compliance with EU MDR. Collaborate across teams to support CE marking processes and uphol...

Transform your career with a pivotal role in Patient Safety & Pharmacovigilance compliance, overseeing QMS, training, and regulatory alignment to enhance product safety and quality across functions. D...