Associate Director Global Regulatory Affairs
MRINetwork
Associate Director, Global Regulatory Affairs
We are seeking an experienced Associate Director for our Global Regulatory Affairs team within our Life Sciences Division. The successful candidate will have a proven track record on filing and liaising with regulatory authorities, specifically the US Food and Drug Administration and European Medicines Agency including Medicines & Healthcare Products Regulatory Agency of the United Kingdom. Experience in Oncology or new therapeutic modalities is preferred. As the Associate Director, you will provide expert guidance in the following key areas:
- Submissions for regulatory applications, including Investigation New Drug, New Drug Application or Biological License Application
- Reviewing archived regulatory applications and assessing any clinical hold issues
- Coordinating and submitting requests for regulatory meetings and interacting with regulatory authorities
- Leading the development and submission of regulatory expedited programs
The ideal candidate will have:
- Advanced degree in life sciences from an accredited institution
- Minimum 3-5 years of pharmaceutical industry experience
- Hands-on experience in regulatory submissions and interactions with regulatory authorities
- Experience in regulatory expedited programs for new therapeutic modalities is a plus
- Strong communication skills and a scientifically driven mindset
- Entrepreneurial mindset and passion for building successful assets
- Excellent analytical and problem-solving skills, with the ability to work well under pressure
- Strong leadership ability, including flexibility and innovation
- Ability to represent the organization as a regulatory affairs expert and to influence in a matrix environment
- Proficiency in solving problems with superior judgment, and the ability to act with grace and resilience under pressure
The position requires flexible working hours, with the ability to travel (international or domestic), and the expectation to be office-based when not travelling.
$154.4k - $242.55k
...Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program... .... Accountabilities: The Associate Director will be responsible for complex... ...concepts within regulatory affairs and implications across the organization...SuggestedMinimum wageFull timeTemporary workLocal areaImmediate startRemote work$154.4k - $242.55k
...boundaries of what is possible in order to bring life-changing therapies to patients worldwide. This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of...SuggestedMinimum wageTemporary workLocal areaImmediate startRemote workWorldwide- ...Associate Director, Global Regulatory Affairs, Advertising and PromotionJob DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients worldwide.The Associate Director, Global Regulatory...SuggestedFull timeRemote workWorldwide
$154.4k - $242.55k
...boundaries of what is possible in order to bring life-changing therapies to patients worldwide. This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of...SuggestedMinimum wageFull timeTemporary workLocal areaRemote workWorldwide$154.4k - $242.55k
...push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director, Global Regulatory Affairs Marketed Products you will: Lead/Contribute global strategies to maximize global regulatory success towards achievement...SuggestedMinimum wageTemporary workLocal areaImmediate startRemote workWorldwide$177k - $278.08k
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...boundaries of what is possible in order to bring life-changing therapies to patients worldwide. This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of...Minimum wageFull timeTemporary workLocal areaImmediate startRemote workWorldwide$222k - $370k
...the development of appropriate regulatory strategies and execution for... ...Accountable to the Global Regulatory Strategy TG Head and... ...required Regulatory Work Package(s) associated with the IES. Capable of providing... ...experience in regulatory affairs (10+ years) ~5 + years...Local area- ...Head of Global Regulatory Advertising and Promotion About the Company Industry shaping biopharmaceutical company Industry Biotechnology Type Public Company About the Role The Company is seeking a Head of Global Regulatory Advertising and Promotion...
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...Provides critical support in developing global regulatory strategy, planning and execution of... ...requirements and provides an assessment of the associated regulatory challenges to the GRL,... ...2 years' experience in regulatory affairs or related areas (e.g., clinical development...Temporary workWork at officeLocal areaFlexible hours$150.2k - $225.3k
...In this role you will report to a Senior Director and join a highly collaborative, patient-focused... ...turns complex medical insight into clear global plans. You will help set the direction for pre- and post-launch medical affairs, ensuring evidence generation, scientific...Temporary workWork at officeLocal areaWorldwideFlexible hours- ...A leading global biopharmaceutical company is seeking an Associate Director, Global Labeling Lead to manage labeling strategies for multiple products. The role requires... ...should possess a strong understanding of regulatory requirements in the US and EU. This position offers...Remote work
$154.4k - $242.55k
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