A company is looking for a Senior Associate Regulatory Information Management. ...
Associate Director, Analytical Regulatory Sciences, Systems & Operations in CMC Regulatory Affairs. The Associate Director, Analytical Regulatory Science, collaborates with product. By balancing analytical knowledge and evolving regulatory expectations with manufacturing and analytical flexibili...
A company is looking for a Quality Associate Director of Regulatory Intelligence. ...
As an Associate General Counsel in the Litigation and Regulatory Practice Group, you will report to the Head of the practice group (who is based in San Jose), and work closely with all members of the Global Legal team and business leaders throughout the company. The right candidate will have a basic...
Associate Director, Regulatory Affairs Advertising and Promotion page is loaded Associate Director, Regulatory Affairs Advertising and Promotion Bewerben locations United States - California - Foster City time type Full time posted on Vor 11 Tagen ausgeschrieben job requisition id R0040533 For Curre...
This role’s primary responsibility is to partner with Regulatory therapy area leadership in obtaining and maintaining regulatory filings and registrations for domestic and international regions. This Associate Director will coordinate activities with internal team members and external parties (e. Ma...
A law firm in Mountain View, CA, is seeking a Senior Health Care Regulatory Associate Attorney with 3+ years of experience in health care regulatory matters. Senior Health Care Regulatory Associate Attorney. Intellectual Property Associate – Trademark, Copyright, Advertising and Media AssociateSan F...
Title: Regulatory Affairs Associate - II*. Analyzed and adapted to scientific and regulatory developments, implementing strategic adjustments in response to the global regulatory landscape. Facilitated cross-departmental collaborations, enhancing the efficiency and timeliness of regulatory submissio...
Collaborate closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Pharmacovigilance, and Quality Assurance, to support regulatory submissions and responses to regulatory agencies. They are seeking a highly skilled and experienced an Associate Director OR Director, ...
Position Title: Regulatory Affairs CMC – Data Administrator Contractor. Work collaboratively to support the RA CMC team to meet deliverables and timelines by executing routine data entry, quality control of that data entry and associated reports. Work is performed under the general supervision of mo...
Experience with regulatory submissions and maintaining regulatory documents. ...
Regulatory Affairs Associates (Data),. Job Title: Regulatory Affairs Associates (Data). Work collaboratively to support the RA CMC team to meet deliverables and timelines by executing routine data entry, quality control of that data entry and associated reports. Work is performed under the general s...
The Associate Director, Medical Writing (Regulatory) will collaborate with colleagues to write high-quality, strategically aligned medical-writing deliverables supporting the regulatory requirements of a clinical development program, ensuring completeness, accuracy, and compliance with US and ex-US ...
Regulatory Affairs CMC – Data Administrator Contractor. Work collaboratively to support the RA CMC team to meet deliverables and timelines by executing routine data entry, quality control of that data entry and associated reports. Work is performed under the general supervision of more senior Regula...
Well versed in ICH guidelines for regulatory submissions (INDs/CTAs/BLAs/MAAs) and associated regulatory documents including clinical protocols/study reports and investigator brochures. Director, Head of Global Regulatory Portfolio Management, with a dotted line reporting to the Interim Head of Medi...
Significant experience contributing to the development of commercial regulatory or related strategies, leading cross-functional regulatory activities, and representing Regulatory to cross-functional teams for multiple products. Regulatory Advertising and Promotion (RA Ad/Promo) is a core function wi...
The Associate Director, Analytical Regulatory Science, collaborates with product. By balancing analytical knowledge and evolving regulatory expectations with manufacturing and analytical flexibility the incumbent will support “right first time” global approvals for CMC control strategies and maintai...
Associate Director, Regulatory Affairs Advertising and Promotion page is loaded Associate Director, Regulatory Affairs Advertising and Promotion Bewerben locations United States - California - Foster City time type Full time posted on Vor 11 Tagen ausgeschrieben job requisition id R0040533 For Curre...
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...
Significant experience contributing to the development of commercial regulatory or related strategies, leading cross-functional regulatory activities, and representing Regulatory to cross-functional teams for multiple products. Regulatory Advertising and Promotion (RA Ad/Promo) is a core function wi...
Regulatory Affairs Associate . ...
The RA Associate Director, Labeling will be overall responsible for ensuring compliance with US regulatory requirements for labeling, and for coordinating internal labelling activities and processes for regulatory submissions and product maintenance. The Regulatory Affairs (RA) Associate Director, L...
The Associate Director, Analytical Regulatory Science, collaborates with product. By balancing analytical knowledge and evolving regulatory expectations with manufacturing and analytical flexibility the incumbent will support “right first time” global approvals for CMC control strategies and maintai...
The Associate Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. May mentor and potentially supervise other regulatory professionals working on the project team and regulatory process-...
Well versed in ICH guidelines for regulatory submissions (INDs/CTAs/BLAs/MAAs) and associated regulatory documents including clinical protocols/study reports and investigator brochures. Director, Head of Global Regulatory Portfolio Management, with a dotted line reporting to the Interim Head of Medi...