Senior Clinical Data Manager

Revolution Medicines is seeking a Senior Clinical Data Manager to lead the clinical data management efforts for our innovative drug development programs. In this pivotal role, you will ensure the accuracy, integrity, and security of clinical data while collaborating with cross-functional teams. Your expertise will help drive the successful execution of clini…

Revolution Medicines is seeking a highly experienced and dynamic Senior Director of Clinical Data Management. In this pivotal role, you will oversee and enhance our clinical data management processes, ensuring the highest standards of data integrity and compliance. You will lead a talented team dedicated to supporting the clinical development of our innovative oncology therapies.Your expertise will be crucial in shaping our data strategy, implementing cutting-edge technologies, and fostering collaborations with cross-functional teams. Join us in our mission to transform cancer treatment!

Position OverviewRevolution Medicines, Inc. is seeking an experienced and strategic Director of Clinical Data Management to lead our data management efforts in clinical trials. In this pivotal role, you will oversee the planning, development, and execution of data management strategies to ensure high-quality and timely delivery of clinical data. Your expertise will contribute to the advancement of our innovative therapies.Key ResponsibilitiesLead and manage the clinical data management team, ensuring adherence to timelines and regulatory requirements.Develop and implement data management processes, including data collection, cleaning, and validation.Collaborate with cross-functional teams to support clinical trial operations.Provide oversight for external vendors involved in data management activities.Ensure compliance with industry standards and best practices in data management.

Join Revolution Medicines, Inc. as a Senior Clinical Program Manager, where you'll lead and oversee pivotal clinical programs that drive innovative cancer therapies from inception through execution. This role will involve collaborating with cross-functional teams to ensure alignment, efficiency, and adherence to regulatory standards while managing timelines and resources effectively.

Revolution Medicines, Inc. is seeking a talented and experienced Senior Clinical Program Manager to join our innovative team in Redwood City, California. In this pivotal role, you will lead and manage clinical program strategies, ensuring the successful execution of clinical trials that align with our mission to transform the lives of patients with cancer.As a Senior Clinical Program Manager, you will collaborate with cross-functional teams, oversee project timelines, and ensure adherence to regulatory requirements. Your expertise will contribute to the advancement of our clinical programs and the development of cutting-edge therapies.

About the RoleWe are seeking a highly skilled and experienced Senior Manager of Clinical Business Systems to lead our dynamic team at Revolution Medicines. In this pivotal role, you will be responsible for overseeing the development and implementation of clinical business systems that ensure the efficiency and effectiveness of our clinical operations.Key ResponsibilitiesDesign, develop, and manage clinical business systems to support clinical trial operations.Collaborate with cross-functional teams to integrate clinical system solutions that enhance data quality and regulatory compliance.Provide leadership and mentorship to team members, fostering a culture of innovation and continuous improvement.Monitor industry trends and technologies to identify opportunities for system enhancements.

Contract Clinical Data Manager Adverum Biotechnologies, Inc. is hiring a Clinical Data Manager (contract) in Redwood City, CA. This role focuses on managing clinical data to support therapies in development. What You Will Do Oversee collection and management of clinical trial data Monitor data quality and accuracy throughout studies Work closely with cross-functional teams to support ongoing trials About the Team Join a group dedicated to advancing innovative therapies. Collaboration and attention to detail are valued here.

Adicet Bio, Inc. is seeking a Senior Clinical Trial Manager to lead the planning and execution of clinical trials in a dynamic and collaborative environment. In this role, you will oversee all aspects of clinical trial management, ensuring compliance with regulatory requirements while achieving project milestones and objectives.

Revolution Medicines is seeking a dynamic and experienced Senior Manager of Clinical Supply Chain to lead our supply chain operations for clinical trials. In this pivotal role, you will oversee the planning, execution, and management of clinical supplies, ensuring that our innovative therapies are delivered on time and within budget. You will work closely with cross-functional teams to develop strategies that enhance operational efficiency and meet regulatory requirements.

Join N-Power Medicine, where we are revolutionizing drug development by reimagining the clinical trial process. Our mission is to enhance the integration of clinical practice and ensure that physicians and patients participate more fully in clinical research. We are building a dynamic, multi-disciplinary team that embodies our core values of community empowerment through generosity, curiosity, and humility. Our urgent goal is to deliver advanced therapies to patients more rapidly.We are currently seeking a motivated Clinical Data Scientist to take ownership of the final stage of our clinical data pipeline. You will play a critical role in transforming intricate datasets from manual abstraction, AI models, and electronic sources into high-quality, analysis-ready deliverables for our pharmaceutical partners. This position is at the crossroads of data science and clinical research, requiring proficiency in data cleaning, transformation, and statistical programming (R, Python, SQL) to create comprehensive reports while ensuring data integrity, accuracy, and compliance with regulatory standards.The ideal candidate will work collaboratively with Clinical Operations, AI Engineers, and Data teams to validate outputs, automate workflows, and enhance our data infrastructure, all while maintaining stringent documentation and adhering to privacy regulations. Proficiency in a Posit development environment and familiarity with GitHub and Jira are essential; experience with Databricks and AI development tools is a plus.This role is perfect for a detail-oriented, technically adept professional with 2-5+ years of experience in clinical data science or related fields, eager to contribute to the acceleration of drug development within a mission-driven and rapidly growing environment.

For over 25 years, Corcept Therapeutics has been dedicated to understanding the science of cortisol, a critical hormone linked to various diseases when imbalanced.Our innovative commercial portfolio includes treatments for conditions such as hypercortisolism and oncology. We have pioneered over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With ongoing advanced clinical trials targeting hypercortisolism, solid tumors, ALS, and liver disease, Corcept is at the forefront of cortisol modulation research to combat some of today's most challenging health issues.Headquartered in Redwood City, California, we invite you to learn more at www.corcept.com.The Senior Clinical Trial Manager (Sr. CTM) will be instrumental in developing and enhancing Corcept’s clinical operations processes and SOP framework. This role includes the independent management of clinical study operations. The Sr. CTM will collaborate with cross-functional teams, vendors, clinical sites, and CROs to ensure protocol adherence and achieve study deliverables, milestones, and objectives within specified timelines and budgets. This is a hybrid position requiring on-site presence three days a week.

About KariusKarius, Inc. is a pioneering life science company specializing in clinical metagenomics, dedicated to enhancing patient care through cutting-edge microbial insights. We strive to revolutionize diagnostic science and technology to improve the diagnosis and treatment of infectious diseases. Leveraging genomics and artificial intelligence, we aim to transform the diagnostic landscape for infectious diseases. Our innovative platform offers unparalleled diagnostic insights by detecting microbial cell-free DNA in the bloodstream, enabling physicians to make swift and informed treatment decisions. Position SummaryAs a Senior Clinical Research Associate, you will oversee clinical site management and monitoring activities to ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and relevant regulations. This role involves performing both on-site and remote monitoring, reviewing monitoring reports and site data for quality and trends, aiding in issue identification and resolution at the site level, and collaborating closely with the clinical study team. The Senior CRA may also mentor junior CRAs, sharing best practices to ensure high-quality monitoring and successful execution of clinical trials. Why Should You Join Us?Join Karius as we tackle infectious diseases through innovations in genomic sequencing and machine learning. Our platform is currently delivering groundbreaking insights into the microbial landscape, equipping clinicians with a comprehensive test that identifies over a thousand pathogens directly from blood, thus accelerating the development of therapeutic solutions across the industry. The advanced products we offer empower physicians to provide better care to patients who have previously been inadequately treated. You will witness firsthand how your contributions can have a life-changing impact on patients at scale. Reports to: Director, Clinical Operations

Role Overview Revolution Medicines is seeking a Clinical TMF Manager to join the Clinical Operations team in Redwood City, California. This role manages Trial Master File (TMF) processes for clinical trials, ensuring all documentation meets regulatory requirements and industry standards. What You Will Do Oversee TMF activities for ongoing and future clinical studies. Monitor TMF compliance with applicable regulations and internal guidelines. Work closely with cross-functional teams to maintain accurate and complete trial documentation. Support the success of clinical programs by ensuring timely and organized TMF management.

Revolution Medicines, Inc. is seeking a highly motivated and organized Clinical Program Manager to oversee our clinical trial initiatives. In this role, you will be pivotal in managing the planning, execution, and reporting of clinical programs, ensuring adherence to regulatory standards and timelines.The ideal candidate will have a strong background in clinical project management, excellent communication skills, and the ability to work collaboratively with cross-functional teams. You will lead project teams, coordinate with external vendors, and facilitate effective communication between stakeholders.

Revolution Medicines is seeking a dynamic and experienced Senior Director of Clinical Development to join our innovative team. In this pivotal role, you will lead and advance our clinical development strategy, overseeing the progression of our groundbreaking therapies from concept through to clinical trials. Your expertise in clinical research and development will be crucial in driving our mission to deliver transformative medicines to patients in need.

Revolution Medicines is at the forefront of clinical oncology, dedicated to developing innovative targeted therapies for patients afflicted with RAS-addicted cancers. Our cutting-edge R&D pipeline features a range of RAS(ON) inhibitors aimed at targeting various oncogenic RAS protein variants, including daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127, all currently advancing through clinical development. As a member of our dynamic team, you will join fellow professionals committed to making a meaningful impact on the lives of patients battling cancers linked to the RAS signaling pathway.The Opportunity:We are on the lookout for a seasoned clinical science drug developer to take on the role of Senior Director of Clinical Development, pivotal in supporting our clinical-stage molecules. In this essential position, you will oversee various clinical science deliverables, ensuring the effective execution of the clinical development plan for specific molecules within their respective indications. Your responsibilities will encompass early-stage clinical research through to pivotal studies, including regulatory submissions. You will play a crucial role in shaping the clinical science component of the Clinical Development Plan (CDP) strategy, driving the advancement of transformative therapies for patients.Lead the clinical science elements of the clinical development strategy and documentation.Represent the clinical development plans across relevant teams, ensuring effective training for study site personnel, acting as the main point of contact for inquiries related to the CDP at a program level, and overseeing medical/safety data reviews and study reporting.Potential assignment to complex and high-priority strategic studies for our molecules, with the expectation of exercising independent and self-directed leadership.Align cross-functionally with scientific, regulatory, and commercial objectives while executing the clinical development plan.Lead, mentor, and contribute to a high-performing cross-functional team of clinical development professionals, fostering a culture of collaboration, innovation, and excellence.Oversee all facets of clinical trial design and execution, including site selection, patient recruitment, data management, and regulatory compliance.

Join SB Energy as a Senior Manager of Contracts for our Data Center division. In this pivotal role, you will oversee contract negotiations, ensuring compliance and alignment with company objectives. You will collaborate closely with cross-functional teams to enhance operational efficiencies and drive strategic initiatives within our data center operations.

Join Revolution Medicines, a pioneering biotechnology company, as a Clinical Program Manager. In this vital role, you will oversee the planning, execution, and management of clinical programs, collaborating with cross-functional teams to drive the development of innovative therapies. Your leadership will be instrumental in advancing our mission to transform the treatment landscape for patients with cancer.

SB Energy develops, owns, and operates large-scale energy and data center infrastructure projects across the United States. Backed by SoftBank and Ares, the company has expanded since 2019 to manage over 3 gigawatts in operation, with a robust pipeline of additional projects nationwide. SB Energy uses advanced technology, including an AI-driven digital platform, to deliver reliable and affordable energy for growing demand. With headquarters in Redwood City, CA, and offices in Denver, CO and San Diego, CA, SB Energy focuses on accelerating the shift to cleaner, more sustainable energy sources. The company emphasizes innovation, teamwork, and strong execution to shape the future of energy and technology. Role overview The Senior Manager, Data Center Controls Engineering, leads the design, standardization, and deployment of control systems for data center projects. This position ensures that Building Management Systems (BMS), Electrical Power Monitoring Systems (EPMS), and related controls infrastructure are scalable, reliable, and fully integrated to support high-performance, mission-critical operations. Beyond technical oversight, this role manages and develops a team of controls engineers. The Senior Manager is responsible for maintaining consistency, quality, and ongoing improvement across a growing portfolio of data center campuses. Location Redwood City, CA; Denver, CO; San Diego, CA; or remote.

Join Revolution Medicines as a Senior Medical Director of Early-Stage Clinical Development, where you will lead our innovative clinical programs aimed at the treatment of cancer. This is an exciting opportunity for a dynamic leader to make a significant impact in the clinical landscape.In this pivotal role, you will oversee the design, implementation, and management of early-stage clinical trials. Your expertise will guide teams in executing clinical strategies and ensuring compliance with regulatory standards.