Associate Director of Clinical Finance

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 an…

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.

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 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.

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.

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.

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.

Revolution Medicines, Inc. seeks an Associate Director, Biostatistics to guide statistical planning and analysis for early-phase clinical trials. Based in Redwood City, California, this position shapes the statistical approach for studies aimed at developing new cancer treatments. Role overview This position leads the design and execution of statistical strategies for early-stage clinical programs. The Associate Director works closely with cross-functional teams to ensure that data from clinical trials is accurate and reliable, supporting the company’s research goals in oncology. Key responsibilities Develop and oversee statistical analysis plans for early-phase clinical studies. Ensure data quality, integrity, and accuracy throughout the clinical development process. Contribute to advancing new cancer therapies by providing statistical expertise. Location This role is based in Redwood City, California.

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

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.

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 Revolution Medicines, Inc. as an Associate Director of Clinical Pharmacology, where you will play a pivotal role in advancing our drug development programs. Collaborate with a dynamic team of professionals to design, implement, and oversee clinical pharmacology studies that contribute to our innovative therapeutic solutions.

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 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 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.

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!

Corcept Therapeutics has been at the forefront of cortisol research for over 25 years. This potent hormone, when unregulated, can significantly impact various diseases. Our innovative commercial portfolio features treatments targeted at hypercortisolism and oncology, and we have pioneered over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. Currently, we are advancing clinical trials focused on hypercortisolism, solid tumors, ALS, and liver diseases, aiming to harness the therapeutic potential of cortisol modulation to combat some of the most challenging health conditions facing patients today.As a Medical Director at Corcept, you will play a pivotal role in the ongoing and upcoming ALS trials, while also contributing to the selection of new indications and the planning of clinical development for Neurology.

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.