Director of Regulatory Affairs

Revolution Medicines, Inc. is seeking a passionate and experienced Director of Regulatory Affairs to lead our regulatory strategy and ensure compliance with all regulatory requirements. In this pivotal role, you will oversee the development and execution of regulatory submissions, manage interactions with regulatory agencies, and guide our product developmen…

Revolution Medicines is hiring a Director of Regulatory Affairs based in Redwood City, California. This position leads regulatory strategy and ensures compliance with global requirements for the company’s therapies. Role overview The Director will manage all interactions with regulatory agencies and oversee the preparation and submission of filings for new and existing therapies. This work supports the advancement of clinical development programs and helps maintain alignment with international standards. Key responsibilities Lead regulatory strategy across multiple programs Ensure all activities comply with global regulations Oversee preparation and submission of regulatory documents Manage communications with regulatory authorities Collaborate with cross-functional teams to drive regulatory initiatives Collaboration This role works closely with teams across clinical development, supporting projects from early-stage research through later phases. The Director plays a central part in shaping regulatory approaches for innovative therapies.

Revolution Medicines is seeking an experienced and strategic Director of Regulatory Affairs to lead our regulatory strategy and operations. In this pivotal role, you will oversee all aspects of regulatory submissions and interactions with health authorities while ensuring compliance with applicable regulations and guidelines. You will collaborate closely with cross-functional teams to align our regulatory approach with organizational objectives and support the advancement of innovative therapies.

Revolution Medicines, Inc. is seeking a highly skilled and motivated Director of Regulatory Affairs to lead our regulatory strategies and submissions. In this pivotal role, you will be responsible for ensuring compliance with all regulatory requirements and facilitating the approval of our innovative therapies. Your expertise will guide our teams in navigating the regulatory landscape, ultimately contributing to our mission of transforming the lives of patients with cancer.

Revolution Medicines is seeking a highly experienced and strategic Director of Regulatory Affairs - Global Filing Lead to oversee regulatory submissions and ensure compliance with global standards. In this critical role, you will lead the regulatory strategy for our innovative drug development programs, engaging with health authorities to facilitate timely approvals. The ideal candidate will possess a deep understanding of regulatory pathways and experience in managing complex submissions.

We are seeking a dynamic and experienced Director of Regulatory Affairs to lead our US filing efforts at Revolution Medicines. In this pivotal role, you will be responsible for overseeing the regulatory strategy and submissions for our innovative therapies, ensuring compliance with FDA requirements. Your leadership will guide cross-functional teams to navigate complex regulatory landscapes, driving our mission to deliver breakthrough medicines to patients.

With over 25 years of commitment to cortisol science, Corcept Therapeutics is at the forefront of developing innovative treatments targeting hypercortisolism and various oncology indications. Our extensive portfolio is powered by over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. As we advance clinical trials in patients suffering from hypercortisolism, solid tumors, ALS, and liver disease, we are dedicated to harnessing cortisol modulation to combat some of the most challenging health conditions today.Located in Redwood City, California, Corcept invites you to explore more about us at www.corcept.com.We are seeking a highly skilled Director of Regulatory Affairs CMC to lead the preparation of CMC regulatory documents from pre-IND to marketing authorization submissions across multiple therapeutic areas, molecules, and regions. This leadership role will guide the CMC regulatory team, ensure compliance with evolving regulations, and spearhead regulatory intelligence initiatives. The position operates in a hybrid format, typically requiring three days on-site each week.

Join Revolution Medicines as the Director of Global CMC Regulatory Affairs, where you will lead the strategic direction and execution of regulatory submissions and compliance for our innovative product pipeline. You will collaborate with cross-functional teams to ensure successful product development and market access.

Revolution Medicines is seeking a highly skilled Director of Regulatory Affairs to lead our US filing initiatives. In this pivotal role, you will be responsible for developing and implementing regulatory strategies that ensure our innovative therapies meet compliance standards and achieve timely market access. You will collaborate closely with cross-functional teams to navigate the regulatory landscape and drive our product development forward.

Revolution Medicines, Inc. is hiring a Director of Global Regulatory Affairs Project Management in Redwood City, California. This leadership role shapes regulatory strategy and manages projects that support the development and approval of new therapies. Key Responsibilities Lead regulatory project management activities for global markets. Oversee compliance to ensure all regulatory requirements are met. Advance initiatives that support the company’s therapeutic pipeline. Location This position is based in Redwood City, California, United States.

Revolution Medicines, Inc. is seeking a highly accomplished Senior Director to lead our Early Development Regulatory Affairs team. In this pivotal role, you will be responsible for shaping regulatory strategies for our innovative oncology programs, ensuring compliance with all regulatory requirements while advancing our mission to transform the lives of patients.The ideal candidate will possess extensive experience in regulatory affairs within the pharmaceutical or biotechnology sectors, with a proven track record of successful submissions and interactions with health authorities. You will collaborate closely with cross-functional teams, including clinical, preclinical, and commercial, to drive our development efforts forward.

Revolution Medicines is seeking a dynamic and experienced Director of Regulatory Affairs to lead our global filing initiatives. As a pivotal member of our regulatory team, you will be responsible for developing and executing regulatory strategies that align with our commitment to bringing innovative therapies to patients.The ideal candidate will have a proven track record in regulatory affairs, with a deep understanding of global regulatory requirements and processes. You will collaborate closely with cross-functional teams to ensure compliance and drive successful submissions.

Join Revolution Medicines as a Regulatory Affairs Intern and gain hands-on experience in the dynamic field of regulatory compliance within the biopharmaceutical industry. This internship will provide you with the opportunity to work alongside industry professionals, contributing to the development and submission of regulatory documents while learning best practices in regulatory strategies.

Join Revolution Medicines, Inc. as a Manager of Regulatory Affairs, where you will play a pivotal role in shaping the regulatory strategy for our innovative therapies. In this dynamic position, you will oversee submissions to regulatory authorities, ensure compliance with regulations, and collaborate closely with cross-functional teams to drive project success.

Revolution Medicines is seeking an experienced and strategic Associate Director of Global Regulatory Affairs Project Management. In this pivotal role, you will lead the planning and execution of regulatory activities for innovative therapeutics, ensuring compliance with global regulations while driving project success. You will collaborate closely with cross-functional teams to develop and implement regulatory strategies that align with our mission of transforming the lives of patients with cancer.

Join Revolution Medicines as a Senior Manager in Regulatory Affairs, where you will play a critical role in guiding our regulatory strategies and ensuring compliance with industry standards. You will lead a team of professionals dedicated to advancing innovative therapies for patients with cancer. This position offers the opportunity to shape the future of our regulatory processes and contribute to groundbreaking research.

Revolution Medicines is seeking a highly motivated and experienced Therapeutic Area Head for Regulatory Affairs to lead our regulatory strategy and compliance for our innovative therapeutic solutions. In this pivotal role, you will be responsible for overseeing regulatory submissions and interactions with health authorities, ensuring that our products meet all necessary regulatory requirements.The ideal candidate will possess a robust understanding of the drug development process, a proven track record in regulatory affairs, and the ability to effectively communicate with cross-functional teams. You will play an integral role in driving our mission to deliver groundbreaking therapies to patients in need.

Revolution Medicines, Inc. is seeking a highly experienced Senior Manager of Commercial Regulatory Affairs to lead our regulatory strategy and ensure compliance with FDA regulations and other relevant guidelines. The ideal candidate will possess a deep understanding of regulatory affairs within the pharmaceutical industry, with a proven track record of managing successful submissions and interactions with regulatory authorities.In this role, you will collaborate with cross-functional teams to align regulatory strategies with commercial objectives and provide expert guidance on regulatory requirements throughout the product lifecycle. You will also be responsible for training and mentoring junior team members, fostering a culture of compliance and excellence within the department.

Revolution Medicines, Inc. is seeking an experienced and dynamic Vice President of Global CMC Regulatory Affairs to lead our regulatory strategy and execution for our innovative drug development programs. This pivotal role will involve overseeing regulatory submissions and ensuring compliance with global CMC regulations, while collaborating closely with cross-functional teams to drive our mission of delivering transformative therapies to patients.

Revolution Medicines, Inc. is seeking a visionary Vice President of Regulatory Science to lead our regulatory strategy and ensure the successful development and approval of innovative therapies. In this pivotal role, you will be responsible for overseeing all regulatory activities, including submissions to health authorities, compliance with regulations, and providing strategic guidance to cross-functional teams. Your expertise will be crucial in navigating the complexities of the regulatory landscape and fostering relationships with regulatory agencies.