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Associate Director, Oncology Regulatory Strategy
2 months ago
We are seeking an experienced Associate Director to lead our Oncology Regulatory Strategy team at GlaxoSmithKline. As a key member of our regulatory affairs team, you will be responsible for developing and implementing regional regulatory strategies to support the development and launch of our oncology products.
Key Responsibilities- Develop and implement regional regulatory strategies to support the development and launch of 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, medical, and clinical, to ensure alignment and effective communication
- Provide regulatory guidance and support to project teams to ensure compliance with regulatory requirements
- Stay up-to-date with regulatory developments and trends in the oncology space and provide insights to inform business decisions
- Bachelor's degree in 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 interpersonal skills, with the ability to work effectively with cross-functional teams
- Strong analytical and problem-solving skills, with the ability to navigate complex regulatory environments
- PhD in Biological or Healthcare Science
- Experience leading regulatory affairs teams or projects
- Knowledge of global and regional regulatory requirements, including FDA and EMA regulations
- Experience with clinical trial and licensing requirements in major countries
At GlaxoSmithKline, we offer a competitive salary and benefits package, as well as opportunities for professional growth and development. We are committed to creating a diverse and inclusive work environment that values and respects the contributions of all employees.