A company is looking for a Regulatory Affairs Director - Global Regulatory Leader (General Medicine/Cardiovascular). ...
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...
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. ...
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...
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, 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 Senior Director, Regulatory Affairs is a key leadership position responsible for developing and executing regulatory strategies and operations necessary to guide the company's products through development, approval, and post-approval phases. Reporting to SVP, Regulatory Affairs and Quality Assur...
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 (Strategy, I&I) to join the Regulatory team. This position works cross-functionally with regulatory affairs and clinical development organizations to facilitate the completion of regulatory filing documentation according to company timelines. The successful candidate wil...
This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings. The position involves developing regulatory strategies, managing submissions, and maintaining communication with regulatory agencies and project teams. Lead gl...
Vir Biotechnology is seeking an a highly motivated, self-driven and enthusiastic Senior Director of Regulatory CMC accountable for ensuring all assigned products have a successful regulatory CMC strategy for clinical development and commercialization. This position will work closely with the Technic...
We are seeking a highly experienced Director of Regulatory Affairs for CMC to oversee and lead regulatory strategies in support of our oncology and immunology therapeutic programs. Director of Regulatory Affairs – Chemistry, Manufacturing, and Controls (CMC). Serve as the primary regulatory contact ...
Director of Regulatory Affairs (San Francisco, CA). This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings. The position involves developing regulatory strategies, managing submissions, and maintaining communication...
The Associate Director, Global Regulatory Affairs provides management of all aspects of assigned regulatory activities for the dedicated regions and related to the development and commercialization of novel liver drugs including quality, preclinical and clinical areas of drug development. In collabo...
The firm is looking for a senior director of fintech legislative and regulatory affairs, for global clients, expanding in the Middle Eastern economies. Preferred field(s) of study: International business legislative and regulatory affairs. The selected candidate will develop Web3 and fintech regulat...
Director of Regulatory Affairs - San Francisco. We are seeking a highly motivated and experienced Senior Director of Regulatory Affairs for a Medical Device Orthopedic Portfolio. Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requireme...
Vir Biotechnology is seeking a highly motivated, self-driven and enthusiastic Senior Director of Regulatory CMC accountable for ensuring all assigned products have a successful regulatory CMC strategy for clinical development and commercialization. This position will work closely with the Technical ...
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...
This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings. The position involves developing regulatory strategies managing submissions and maintaining communication with regulatory agencies and project teams. Lead glob...
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...
Associate Director, Clinical Regulatory Affairs . This successful candidate will be proficient in the principles of scientific writing and will work cross?functionally, advising the team on regulatory expectations for document co...
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...
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...
Thisrole provides global regulatory leadership and expertise to ensurecompliance and successful submission of clinical regulatoryfilings. The position involves developing regulatory strategiesmanaging submissions and maintaining communication with regulatoryagencies and projectteams. Overseethe prep...