Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.
Experience Level
Experience
Qualifications
The ideal candidate will possess a Bachelor's degree in Life Sciences or a related field, with at least 3-5 years of experience in clinical project management. Strong knowledge of GCP and ICH guidelines is required. Excellent communication, organizational, and leadership skills are essential, along with the ability to work effectively in a fast-paced environment.
About the job
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.
About Revolution Medicines, Inc.
Revolution Medicines is dedicated to delivering breakthrough therapies to cancer patients. With a robust pipeline of targeted drug candidates, our team is driven by a passion for innovation and a commitment to improving patient outcomes. We foster a collaborative and inclusive culture where every team member contributes to our shared success.
Full-time|On-site|Redwood City, California, United States
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 …
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|On-site|Redwood City, California, United States
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.
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|On-site|Redwood City, California, United States
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.
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!
As a Senior Program Manager in Vendor Operations at Chan Zuckerberg Initiative, you will play a pivotal role in optimizing our vendor management processes. You will lead strategic initiatives to enhance operational efficiency and ensure the alignment of vendor services with organizational goals. The ideal candidate will leverage their expertise in program management to foster strong relationships with vendors while driving continuous improvement in service delivery.
Full-time|On-site|Redwood City, California, United States
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.
Full-time|$170.5K/yr - $200.7K/yr|Hybrid|Redwood City, California, United States
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.
Full-time|Hybrid|Redwood City, CA (Hybrid) or Remote (USA)
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
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
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|On-site|Redwood City, California, United States
Revolution Medicines, Inc. seeks a Director of Program Management to lead its program management team in Redwood City, California. This position is central to planning, executing, and delivering a range of programs that drive the company’s therapeutics pipeline forward. Key responsibilities Direct multiple programs from early planning stages through to completion, ensuring all milestones are achieved. Coordinate cross-functional teams to maintain alignment and focus across efforts. Oversee timelines, budgets, and resource allocation to support program objectives. Promote clear and consistent communication among stakeholders throughout the organization. Requirements Significant program management experience within the biopharmaceutical sector. Proven ability to lead complex projects that span multiple teams. Strong skills in organization and communication. Role impact This leadership role directly supports Revolution Medicines’ mission to develop new treatments that improve outcomes for cancer patients.
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|$176K/yr - $303.6K/yr|On-site|Redwood City, California, United States
At Carbon, we strive to transcend traditional 3D printing. Our mission is to empower creators globally to produce what the world needs at this moment. Our organization is founded on the belief that diverse disciplines can unite to tackle complex challenges. We have ambitious goals to develop technologies that will reshape industries worldwide. As a member of our inclusive team, you will thrive in a dynamic culture where collective achievements are valued as much as individual contributions. Join us in revolutionizing the world, and we'll help transform yours.In this role, you will co-lead our most significant and high-stakes initiatives, navigating through uncertainty to deliver scalable solutions. You will serve as a strategic partner to engineering leadership, diving deep into technical trade-offs with architects while aligning multi-year roadmaps with executive stakeholders.
Full-time|$190K/yr - $261.8K/yr|Hybrid|Redwood City, CA (Hybrid)
The Chan Zuckerberg Initiative, established in 2015 by Priscilla Chan and Mark Zuckerberg, is dedicated to tackling some of society's most pressing challenges, ranging from disease prevention and cure to enhancing education and meeting community needs. We offer robust operational support across our diverse initiatives.The TeamOur work spans Science, Education, and community engagement, where we integrate technology with grantmaking, impact investing, and collaborative efforts to expedite progress toward our mission. The Operations organization is pivotal in driving this work forward.Our Operations encompass teams in Brand & Communications, Central Tech, Finance, People, Real Estate/Workplace/Events/Facilities/Security (REWFS), Strategy & Operations, and Ventures. These teams deliver essential services, strategies, and operational support needed for CZI to fulfill its mission of creating a better future for all.The OpportunityWe are looking for a talented Technical Program Manager with a focus on Application Security, particularly in identifying vulnerabilities and developing innovative solutions to mitigate those risks at scale. Your role will extend beyond merely fixing security vulnerabilities; you will be instrumental in creating secure frameworks to preemptively address potential issues. You will collaborate closely with developers and engineers across large organizations, utilizing your deep technical knowledge in security and development to establish secure foundations for the application and infrastructure teams supporting the CZI Enterprise.This role will significantly shape product and application security, safeguarding scientific and educational innovation at the Chan Zuckerberg Initiative, Biohub, and Learning Commons. You will partner with a dynamic team of engineers, Product Managers, and Security Professionals to build shared tools and platforms that support a diverse collection of Research Scientists, Data Scientists, AI Researchers, and Engineers working on some of the world’s most intricate challenges. As part of the Information Security team, your contributions will directly influence all of CZI’s initiatives by ensuring the security and scalability of the technological solutions fueling our mission.What You'll DoConceive, design, develop, and improve...
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.
Full-time|On-site|Redwood City, California, United States
Revolution Medicines is seeking a highly motivated and experienced Senior Scientist I for our Clinical Biomarker Development team. In this pivotal role, you will be responsible for the design, execution, and interpretation of biomarker studies aimed at supporting clinical trials. You will work closely with cross-functional teams to advance our innovative therapies and contribute to our mission of transforming the lives of patients with cancer.