Clinical TMF Manager, 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…

Join Revolution Medicines as an Associate Director of Clinical TMF Management, where you will lead a team focused on ensuring the highest quality in clinical trial master file (TMF) management. Your expertise in clinical operations will be crucial in enhancing our processes and compliance.

Role Overview Karius, Inc. is hiring a Director of Clinical Operations to strengthen clinical processes and uphold high standards across services. This leadership role calls for a strategic approach and deep experience in clinical operations. The Director will focus on refining workflows and supporting improved patient outcomes. Location This position is based in Redwood City, CA with a hybrid schedule, or can be performed remotely within the United States.

Join Revolution Medicines, Inc. as an Associate Director of Clinical Operations, where you will play a pivotal role in advancing the development of innovative therapies. This leadership position will involve overseeing clinical trial management, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to drive project success.

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.

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, 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.

We are seeking an experienced and dynamic Associate Director of Clinical Operations to join our team at Revolution Medicines. In this pivotal role, you will lead the planning, execution, and management of clinical trials, ensuring alignment with regulatory guidelines and company objectives. You will work closely with cross-functional teams to deliver innovative therapies to patients.

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 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 clinical trials, ultimately contributing to advancing therapies for patients.

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.

Join Revolution Medicines as an Intern in Clinical Trial Operations and be part of a pioneering team dedicated to advancing innovative therapies for cancer. This is a unique opportunity to gain hands-on experience in clinical operations, collaborate with industry experts, and contribute to impactful projects that aim to bring hope to patients.

The Associate Director of Clinical Operations Compliance & Training at Revolution Medicines focuses on upholding compliance and supporting training programs within clinical operations. This role is based in Redwood City, California. Role overview This position centers on maintaining the integrity of clinical operations by ensuring regulatory standards are met. The Associate Director will guide training efforts and help reinforce consistent practices across teams. Key responsibilities Oversee compliance activities related to clinical operations Lead and coordinate training initiatives for staff Promote adherence to regulatory requirements and internal policies Work environment This role operates within a biotechnology setting where attention to detail and commitment to regulatory standards are essential.

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.

Join Revolution Medicines as an Intern in Clinical Operations Execution Optimization, where you'll gain hands-on experience in optimizing clinical processes. This role will immerse you in the dynamic world of clinical research, allowing you to contribute to our mission of advancing innovative therapies for patients in need.

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.

Join Revolution Medicines as a Clinical Trial Operations Intern and gain invaluable experience in the dynamic field of clinical research. As an intern, you will support the planning and execution of clinical trials, collaborating with cross-functional teams to ensure the success of our innovative drug development programs.

Join Revolution Medicines as the Director of Clinical Supply Chain, focusing on Comparators and External Collaborations. In this pivotal role, you will lead the strategic planning and execution of clinical supply chain operations, ensuring timely delivery of comparator drugs and oversight of external partnerships. You will collaborate with cross-functional teams to optimize our supply chain processes, drive efficiency, and contribute to the advancement of our clinical programs.

Revolution Medicines, Inc. is hiring a Clinical Trial Assistant based in Redwood City, California. This role provides daily support to the clinical operations team, focusing on coordination and management tasks throughout the clinical trial process. The position plays an important part in maintaining compliance with regulatory guidelines and established protocols. Key responsibilities Organize and track activities related to ongoing clinical trials Support documentation and record-keeping to ensure regulatory requirements are met Coordinate communication among internal team members and trial sites Contribute to the accuracy and efficiency of trial operations What we look for Attention to detail in managing trial tasks and records Strong organizational skills for handling multiple responsibilities Dedication to supporting clinical research with a positive impact on patient lives

Revolution Medicines is a pioneering clinical oncology firm at the forefront of developing innovative targeted therapies for patients battling RAS-addicted cancers. Our robust R&D pipeline features RAS(ON) inhibitors aimed at suppressing various oncogenic RAS protein variants. Currently, our RAS(ON) inhibitors in clinical development include daraxonrasib (RMC-6236), a multi-selective inhibitor; elironrasib (RMC-6291), a G12C-selective inhibitor; zoldonrasib (RMC-9805), a G12D-selective inhibitor; and RMC-5127, a G12V-selective inhibitor. As a valued member of our team, you will collaborate with exceptional professionals committed to improving the lives of cancer patients with RAS signaling pathway mutations.The Opportunity:We are seeking a dynamic Clinical Operations Professional with strong leadership abilities, exceptional organizational skills, and deep technical knowledge in clinical drug development. As the Associate Director of Clinical Operations Enablement & Knowledge Systems, you will play a pivotal role within the Clinical Operations Excellence team. Your key responsibilities will include developing and scaling the Clinical Operations knowledge ecosystem—ensuring information is structured, accessible, and effectively utilized to facilitate consistent, efficient, and high-quality study execution across various roles and programs. This role emphasizes execution and aims to enhance the capabilities of the Clinical Operations organization.The ideal candidate is a Clinical Operations leader who merges extensive study execution experience with the talent for creating scalable, user-centered systems that empower team members to excel.Lead the design and implementation of a comprehensive Clinical Operations knowledge ecosystem, inclusive of playbooks, toolkits, and structured resources that assure high-quality study execution.Develop role-specific enablement frameworks that correspond to Clinical Operations responsibilities, study activities, and significant transition points.Design and provide diverse learning solutions (e.g., live sessions, on-demand modules, short-form videos, playbooks, and interactive resources) to optimize accessibility and encourage adoption.Utilize adult learning principles and user-centered design to ensure the content is practical, engaging, and immediately applicable.Incorporate knowledge of Clinical Operations workflows and regulatory requirements (e.g., GCP, ICH) to guarantee that learning content remains relevant, practical, and aligned with real-world study execution.