Associate Director, Oncology Regulatory Strategy
18 hours ago
We are seeking an experienced Associate Director to lead our Oncology Regulatory Strategy team. The successful candidate will be responsible for developing and implementing regional regulatory strategies to support the development and launch of new oncology products.
Key Responsibilities- Develop and implement regional regulatory strategies to support the development and launch of new oncology products.
- Lead interactions with local and regional regulatory authorities to ensure compliance with global and regional requirements.
- Collaborate with cross-functional teams, including commercial and medical affairs, to ensure alignment and effective communication.
- Provide regulatory expertise and guidance to support the development and launch of new oncology products.
- Stay up-to-date with regulatory requirements and trends in the oncology space to ensure our strategies remain effective and compliant.
- Bachelor's degree in a relevant field, such as biological or healthcare science.
- Minimum 5 years of experience in regulatory affairs, with a focus on oncology.
- Proven track record of developing and implementing successful regulatory strategies.
- Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
- Strong knowledge of regulatory requirements and trends in the oncology space.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced regulatory professional looking for a new challenge, we encourage you to apply.
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Collegeville, Pennsylvania, United States GSK Full timeJob SummaryWe are seeking a highly skilled and experienced Associate Director, Oncology Regulatory Affairs to join our team at GSK. As a key member of our regulatory affairs team, you will be responsible for developing and implementing regulatory strategies to support the development and approval of oncology products.Key ResponsibilitiesDevelop and implement...
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Director of Global Regulatory Affairs
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Director of Regulatory Policy and Advocacy
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Medical Director Oncology Clinical Development
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Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeAbout the RoleWe are seeking a highly skilled Medical Director to join our Oncology Clinical Development team at GlaxoSmithKline. As a key member of our team, you will be responsible for leading clinical research activities and advancing the development of our clinical portfolio.Key ResponsibilitiesCollaborate with cross-functional teams to develop and...
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Medical Director Oncology Clinical Development
18 hours ago
Collegeville, Pennsylvania, United States GSK Full timeJob Title: Medical Director Oncology Clinical DevelopmentWe are seeking a highly skilled Medical Director to lead our Oncology Clinical Development team. As a key member of our Clinical Development organization, you will be responsible for developing and executing clinical trials to advance the development of our clinical portfolio.Key...
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Director of Regulatory Affairs CMC
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Regulatory Affairs Director
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Director, Global Regulatory Affairs, Vaccines
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Director of Clinical Pharmacology and Modeling
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Associate Director of Analytical Development
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