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

Director* of Regulatory Affairs. Act as the main point of contact for regulatory authorities, managing all communication, including pre-submissions, Q-subs, and meetings with regulatory bodies. Collaborate with clinical teams on regulatory submissions and trial designs, ensuring compliance with regu...

A company is looking for a Director of Regulatory Affairs, Advertising/Promotion. ...

Associate Director Regulatory Affairs (Temp to Perm). Oversee regulatory submissions and approvals, ensuring alignment with global regulatory standards. Regulatory Affairs, including. Lead regulatory strategy development and execution for both U. ...

A company is looking for an Associate Director, Regulatory Affairs and Submissions. ...

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...

A company is looking for a Regulatory Affairs Director - Global Regulatory Leader (General Medicine/Cardiovascular). ...

Seeking an experienced Director of Regulatory Affairs to join a dynamic Regulatory Affairs team in a hybrid role, with some onsite presence required at our Redwood City, CA offices. Offer strategic regulatory guidance across teams (R&D, clinical, operations, legal, marketing) to align with regulator...

As an Associate Director of Regulatory Affairs, you will represent regulatory affairs on cross-functional teams and provide regulatory advice on clinical development matters. Associate Director, Regulatory Affairs. Regulatory Affairs, regulatory submissions, drug development, oncology, FDA, EMA. Fun...

As the Director of Regulatory Affairs, you will be a pivotal leader within the company, driving strategic regulatory decisions across the entire portfolio. Director of Regulatory Affairs. You’ll co-lead a growing regulatory team, and play a key role within regulatory submission and strategy. Regulat...

Director of Regulatory Affairs, you’ll take the helm of regulatory submissions and strategic planning for successful drug approvals across key markets, including the FDA, EMA, and other regulatory agencies worldwide. Are you ready to lead regulatory strategies that bring innovative therapeutics from...

Director of Regulatory Affairs - Full Time - Onsite/Hybrid/Remote. The Director will work closely and report to the Head of Regulatory Affairs. Work closely with the Head of Regulatory Affairs to achieve company goals. Any other regulatory affairs tasks assigned or required as per the business needs...

This Senior Director/Director of Regulatory Affairs will also oversee the preparation of all regulatory documents and submissions, mentor junior team members, and stay updated on changes in FDA and EU regulations. Senior Director/Director of Regulatory Affairs. Regulatory Affairs experience in a pha...

Primary responsibilities are to support Shell Energy's wholesale/retail trading/origination businesses and Shell Renewable and Energy Solutions related businesses through external advocacy for competitive markets, communicating regulatory changes and impacts of regulatory changes to commercial teams...

The Director, Regulatory Affairs will support the development and execution of domestic and international regulatory strategy for Codera. The Director, Regulatory Affairs is responsible for ensuring documentation is clear and accurate, complies with regulatory requirements, conforms to company quali...

The Associate Director of Regulatory Affairs will play a crucial role in leading and managing the regulatory submissions for CorDx medical device products, including 510(k) and De Novo submissions. Job Title: Associate Director of Regulatory Affairs. Conduct regulatory assessments for product change...

We are in search of an accomplished and dynamic Senior Director of Regulatory Affairs to join our team. Reporting directly to the Chief Medical Officer, the Senior Director will provide strategic leadership, ensuring compliance with global regulatory standards while supporting organizational objecti...

The Senior Director, Regulatory Affairs is responsible for establishing regulatory strategies in coordination with departmental leadership, and independently developing and managing life cycle plans along with regulatory submissions and approvals. Senior Director, Regulatory Affairs . Establish regu...

Director of Regulatory Affairs. You’d oversee regulatory filings, partner with external consultants, and eventually build out the regulatory function internally. Partner with external regulatory consultants and oversee the build-out of the internal regulatory function. This role will be pivotal in b...

Director, Regulatory Affairs will be responsible for developing and executing innovative CMC regulatory strategies in support of the global development and commercialization of a drug/device combination product. Lead global CMC regulatory submission development - responsible for planning, coordinati...

The Executive Director, Regulatory Affairs will develop and execute global regulatory strategic and tactical guidance for the development of innovative new drugs in rare disease ensuring fast to market global product registrations, product promotion, maintenance of products and processes in regulato...

The position is responsible for leading CMC regulatory activities within Regulatory Affairs department, to support all ORIC’s clinical development programs of oncology products. Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ...

Director, Regulatory Affairs is the ranking Regulatory Affairs leader for the Infusion Process Excellence RA organization under the Medication Management Business Unit. This position provides expertise and leadership to business partners, the Associate Director of Process Excellence Regulatory Affai...

The Associate Director of Regulatory Affairs will play a crucial role in leading and managing the regulatory submissions for CorDx medical device products, including 510(k) and De Novo submissions. Job Title: Associate Director of Regulatory Affairs. Conduct regulatory assessments for product change...

Primary responsibilities are to support Shell Energy's wholesale/retail trading/origination businesses and Shell Renewable and Energy Solutions related businesses through external advocacy for competitive markets, communicating regulatory changes and impacts of regulatory changes to commercial teams...

Director* of Regulatory Affairs. Act as the main point of contact for regulatory authorities, managing all communication, including pre-submissions, Q-subs, and meetings with regulatory bodies. Collaborate with clinical teams on regulatory submissions and trial designs, ensuring compliance with regu...