Regulatory Affairs Director: Average Salary in San Francisco, CA in 2024

My client is seeking a Director, Regulatory Affairs to join their Regulatory team. At least 8-10+ years of Regulatory Affairs experience. Be able to prepare nd lead successful regulatory meetings and major health authority interactions. Extensive global regulatory submission experience (IND/CTA/BLA/...

Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory environment. Serve as the Global Regulatory Lead on project teams and key sub-teams. Develop and implement competit...

Director/Senior Director, Regulatory Affairs. They are looking for a Director or Senior Director of Clinical Regulatory Affairs to join their team. Develop and execute Clinical Regulatory Affairs strategies to support clinical development objectives. Minimum 7 years specifically in clinical regulato...

They are looking to bring on a Senior Director, Regulatory Affairs to the team. Provide strategic and operational leadership in regulatory affairs, including regulatory strategies, clinical study requirements, and marketing approvals in various regions. Utilize deep knowledge of regulatory requireme...

As the Regulatory Affairs Director, you will have the opportunity to lead Allogeneic trials – the most innovative in history! This role allows you to bring past Regulatory knowledge to the table, while also be creative in strategic discussions and decisions. Regulatory Affairs experience within a ph...

Director, CMC Regulatory Affairs. Serve as the PDM regulatory representative on project teams, provide CMC regulatory support for the clinical development of the investigational product(s), and ensure applicable regulatory requirements are appropriately met. The position is responsible for providing...

A degree in a life science, chemistry, or chemical engineering or closely related discipline with a graduate degree preferred and at least 10 years of experience in pharmaceutical regulatory affairs, that includes, but cannot be limited to, CMC regulatory affairs. Associate) Director, Regulatory Aff...

Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market. Collaborate with various regulatory consultants, clinical advisory board members, and board members to maintain regulatory knowledge...

Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market. Collaborate with various regulatory consultants, clinical advisory board members, and board members to maintain regulatory knowledge...

Executive Director/Senior Director, Regulatory Affairs. Understands the regulatory environment for pharmaceutical companies, as well as pharmaceutical industry regulatory affairs best practices to satisfy regulatory requirements. Provides regulatory leadership in support of the development, registra...

Establishes processes and measures to monitor conformance with Regulatory Affairs procedures and compliance with regulatory requirements. Interpret regulatory intelligence to assess the impact on Exelixis and advise Regulatory Affairs leadership accordingly. Establish process and measures to ensure ...

We are currently seeking a Regulatory Affairs Associate Director/Director to join our growing regulatory team. Job Title: Global Regulatory Affairs Associate Director/Director. Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, includ...

Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market. Collaborate with various regulatory consultants, clinical advisory board members, and board members to maintain regulatory knowledge...

You will provide regulatory support in development and execution of regulatory strategies in support of the global clinical trial applications, marketing authorizations, and life cycle management of an expanding oncology portfolio in compliance with applicable regulatory requirements. Ensures regula...

We are currently seeking a Regulatory Affairs Associate Director/Director to join our growing regulatory team. Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory envi...

Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market. Collaborate with various regulatory consultants, clinical advisory board members, and board members to maintain regulatory knowledge...

The Regulatory Affairs Director (RAD) provides strategic and operational regulatory leadership to the development, commercialization and life cycle management of assigned oncology products. Would you like to apply your Regulatory Affairs strategy expertise and passion to make an impact in a company ...

Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market. Collaborate with various regulatory consultants, clinical advisory board members, and board members to maintain regulatory knowledge...

Associate Director Regulatory Affairs – US New Product Introduction and On-Market Changes. The individual may monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop regulatory submission strategy, and provide executive mana...

Provides leadership within the Commercial Regulatory Affairs department, identifying and managing through completion departmental and cross-project initiatives and regulatory obligations. Responsible for the regulatory review and approval of scientific exchange materials, including Medical Informati...

As a manager, the function of an Associate Director Regulatory Affairs, APAC (Asia Pacific) is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. Associate Director Regulatory Affairs – A...

Director of Regulatory Affairs. Represent Regulatory Affairs in cross-functional development teams and ensure alignment with regulatory requirements. As the global regulatory lead (GRL), you will work cross-functionally with teams to manage regulatory submissions and approvals, ensuring compliance w...

Lead regulatory strategy, provide regulatory guidance/precedents; identify, assess, and mitigate regulatory risks. Monitor regulatory agency activities in the relevant space and maintain a global perspective on regulatory strategy. Regulatory Affairs in biopharma industry or equivalent. Providing re...

Innova Solutions is immediately hiring for an Associate Director, Regulatory Affairs. Associate Director, Regulatory Affairs , you. In collaboration with Regulatory Affairs functional management, coordinate the provision of resources from the various Regulatory functions in support of clinical studi...

This role requires an extensive knowledge of the roles and responsibilities of Regulatory Affairs spanning both clinical and commercial phases of drug development, and how Regulatory Affairs connects with other functional areas. Has experience specifically in the Regulatory Affairs Global Labeling f...