Principal Regulatory Writer at Apsida Life Science
Apsida Life Science
Elevate your career at Apsida Life Science as a Principal Regulatory Writer, supporting pharmaceutical clients in Canada or the US. Utilize your expertise in regulatory writing to address complex challenges with clarity. Apsida Life Science seeks a Principal Regulatory Writer with over 5 years in Regulatory Writing. This senior role involves leading strategic programs and providing scientific input on CTD Module 2 submissions. Your contributions will be pivotal in expanding the company's footprint in the North American market, working collaboratively across a diverse range of therapeutic areas. Key Responsibilities:
- Serve as the primary contact for project deliverables
- Lead high-complexity submissions, including CTD Module 2
- Ensure clarity in technical documentation and communication
- Collaborate with Project Management on budget development
- Degree in Life Science or related field
- 5+ years of Regulatory Writing experience
- Experience with CTD Module 2 submissions
- Proven background as a Senior/Principal Regulatory Writer
Vacancy posted 3 hours ago
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