Principal Regulatory Writer

Position: Principal Regulatory Writer at Apsida Life Science
Location: Granby

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

Requirements:

• 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

Bring your regulatory expertise to help life sciences thrive at Apsida.
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