Associate Director, Global Regulatory Affairs
Associate Director, Global Regulatory Affairs
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Salary Not Disclosed
1 Vacancy
Job Description
See Yourself at Telix
The Associate Director Global Regulatory Affairs is primarily responsible for ensuring regulatory objectives are met and align with Telixs corporate objectives. This person is responsible for the execution of global regulatory strategy and dossier compliance within Telix specifically for assigned products.
Key Accountabilities:
- Prepares and executes in collaboration with other regulatory affairs team members global regulatory strategies and submission requirements pertaining to assigned projects in line with Telixs objectives and initiatives.
- Represents regulatory affairs on project teams as a subject matter expert by providing guidance and regulatory expertise to other departments in support to product development.
- Leads regulatory agency interactions including but not limited to coordination of redaction of briefing package preparation of meeting minutes and responses to agencies questions.
- Prepares reviews analyses and consolidates all relevant pharmaceutical and related technical information required for regulatory submission of the companys (investigational-) medicinal products with regulatory agencies (ODD PIP/PSP Scientific advices IND/CTA BLA/MAA).
- Provides regulatory assessments for change management and ensures compliance of the regulatory submissions by filing and/or coordinating regulatory amendments in relation to the change where applicable.
- Monitors global health authority regulations guidelines and specifications including FDA EMA Health Canada Therapeutic Goods Authority to maintain regulatory submission compliance.
- Leads regulatory interaction with health authorities for IND and BLA filings (or equivalent).
Education and Experience:
- Undergraduate degree in a scientific field (chemistry biology pharmaceutical sciences) required; Advanced degree preferred
- 9 years experience in regulatory affairs for pharmaceuticals products required
- Direct experience in writing regulatory sections for global health authority applications (i.e. IND/IMPD BLA/MAA)
- Direct experience in Radiopharmaceuticals biologicals and/or clinical preferred
- Experience across product development to Marketing Authorization
- Comprehensive knowledge of drug development process biopharmaceutical technology drug manufacturing processes GMP and related issues.
- Ability to understand and interpret any regional regulations and guidance documents as well as common and scientific publications
- Experience working globally in the US and EMEA
Key Capabilities:
- Inclusive mindset: Demonstrate an understanding and appreciation for diversity and actively work to create an inclusive environment where everyone feels valued and respected
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
- Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
- Results-oriented: Driven to achieve goals and objectives with a strong focus on delivering measurable results
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
- Adaptability: Comfortable working in a dynamic environment able to adjust to changing priorities and willing to take on new challenges
- Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels using clear and concise language
- Collaboration: Work effectively as part of a team actively sharing knowledge and expertise to achieve common goals
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
- Continuous learning: Show a commitment to ongoing learning and professional development continually seeking out opportunities to expand your knowledge and skills
Required Experience:
Exec
Employment Type
Full Time
