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Experience Level
Senior Level Manager
Qualifications
The successful candidate will have a Master's Degree or higher in a relevant field, with a minimum of 5 years of experience in clinical quality assurance or a similar role within the biotechnology or pharmaceutical industry. Proven expertise in regulatory compliance, risk management, and quality systems is essential. Strong leadership and communication skills are necessary to effectively collaborate across multidisciplinary teams.
About the job
Revolution Medicines, Inc. is seeking an experienced and passionate Director of Clinical Quality to spearhead our quality assurance initiatives within our clinical operations. This pivotal role will focus on developing and implementing quality systems that ensure compliance with regulatory requirements and enhance the overall integrity of clinical trials. The ideal candidate will possess a strong background in clinical quality oversight and a commitment to driving continuous improvement in quality standards.
About Revolution Medicines, Inc.
Revolution Medicines, Inc. is a pioneering biotechnology company dedicated to transforming the lives of patients through innovative therapies. Our mission is to harness the power of targeted medicines to treat complex diseases, and we are committed to advancing science and improving patient outcomes.
Full-time|On-site|Redwood City, California, United States
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 experti…
Full-time|On-site|Redwood City, California, United States
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!
Full-time|On-site|Redwood City, California, United States
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.
Full-time|Hybrid|Redwood City, CA (Hybrid) or Remote (USA)
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.
Full-time|On-site|Redwood City, California, United States
Revolution Medicines, Inc. is seeking an experienced and passionate Director of Clinical Quality to spearhead our quality assurance initiatives within our clinical operations. This pivotal role will focus on developing and implementing quality systems that ensure compliance with regulatory requirements and enhance the overall integrity of clinical trials. The ideal candidate will possess a strong background in clinical quality oversight and a commitment to driving continuous improvement in quality standards.
Full-time|On-site|Redwood City, California, 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.
Full-time|On-site|Redwood City, California, United States
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.
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.
Full-time|On-site|Redwood City, California, United States
Revolution Medicines is seeking a highly accomplished and visionary Executive Director of Clinical Development to lead our clinical programs. In this pivotal role, you will spearhead the development and execution of clinical strategies that drive the advancement of our innovative therapies. Your expertise will guide our clinical trials, ensuring they align with regulatory requirements and achieve optimal outcomes.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|$244K/yr - $305K/yr|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
Revolution Medicines is hiring an Associate Director of Clinical Finance based in Redwood City, California. This position shapes the financial direction of clinical operations by managing budgets, forecasts, and financial analysis for clinical development programs. Key responsibilities Oversee the budgeting process for clinical programs, ensuring accuracy and alignment with organizational goals Lead forecasting activities to support both current and upcoming clinical development initiatives Analyze financial data to support informed decision-making and effective resource allocation Offer financial guidance to cross-functional teams throughout the organization Role impact This position plays a central role in making sure resources for clinical research and development are allocated efficiently, directly supporting Revolution Medicines’ work in the biopharmaceutical sector.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
Join Revolution Medicines as an Associate Director of Clinical Development, where you will play a pivotal role in advancing our innovative drug development programs. You will collaborate with cross-functional teams to design, implement, and oversee clinical trials, ensuring exceptional execution and compliance with regulatory standards. Your expertise will contribute to our mission of delivering transformative therapies to patients with cancer.
Full-time|$132K/yr - $226K/yr|Hybrid|Redwood City, CA
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.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
Revolution Medicines, Inc. is seeking an accomplished Executive Director of Clinical Supply Chain to lead our innovative supply chain strategy in the clinical trial landscape. This pivotal role involves overseeing the end-to-end clinical supply chain operations, ensuring timely and efficient delivery of supplies to support our groundbreaking therapeutic developments. The ideal candidate will possess extensive experience in clinical supply chain management, regulatory compliance, and cross-functional leadership.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
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.
