Note: The job is a remote job and is open to candidates in USA. Angitia Biopharmaceuticals is hiring a Senior Manager/Associate Director, Regulatory Writer to lead regulatory writing across its development portfolio. The role plans, authors, coordinates, and delivers regulatory documents from IND through marketing applications and lifecycle management, while providing strategic document leadership and partnering with cross-functional teams.

Responsibilities

• Lead the development of strategic document plans supporting global regulatory submissions and health authority interactions
• Serve as lead writer for complex regulatory documents including: + Protocols and protocol amendments + Investigator's Brochures (IBs) + Clinical Study Reports (CSRs) + Briefing packages + INDs and CTAs + Orphan Drug Designation applications + Pediatric Investigation Plans (PIPs) + Pediatric Study Plans (PSPs) + Annual reports and development updates + Responses to health authority questions
• Develop integrated document strategies that ensure consistency across regulatory, clinical, nonclinical, safety, and CMC content
• Lead document planning and review meetings with cross-functional project teams
• Facilitate alignment among subject matter experts and resolve content issues to maintain timelines and document quality
• Partner closely with Regulatory Affairs to support global regulatory strategies and agency interactions
• Represent Regulatory Writing on project teams and governance meetings
• Develop and maintain writing processes, templates, style guides, and document development standards
• Identify opportunities to improve writing workflows and submission readiness
• Manage external medical writing vendors and contract writers as needed
• Mentor junior writers and contribute to development of organizational writing capabilities
• Coordinate document finalization and publishing activities for major submissions
• Ensure compliance with ICH, FDA, EMA, PMDA, and other applicable regulatory requirements
• Support preparation for regulatory meetings and agency interactions

Skills

• Bachelor's degree in life sciences or related discipline
• Minimum 10 years of medical writing or regulatory writing experience within biotechnology, pharmaceutical, or CRO environments
• Demonstrated experience serving as lead writer for major regulatory documents
• Extensive experience authoring and coordinating: + Protocols + Investigator's Brochures + Clinical Study Reports + Regulatory briefing documents + IND and CTA submissions + Health authority responses
• Strong knowledge of ICH guidelines, Good Clinical Practice (GCP), FDA, EMA, and international regulatory requirements
• Demonstrated ability to independently manage multiple complex writing projects simultaneously
• Experience leading cross-functional teams through document development and review cycles
• Advanced degree (PhD, PharmD, MD, MS) in a scientific discipline
• AMWA certification
• Experience supporting BLA, MAA, or NDA submissions
• Experience in rare disease and pediatric development programs
• Experience supporting biologics development
• Experience managing external writing vendors and consultants
• Bilingual English and Chinese proficiency

Benefits

• Medical, dental, and vision coverage for employees and their eligible dependents
• 401(K) Retirement Plan with Company match
• Company paid Long Term Disability Coverage
• Company-paid life Insurance & AD&D Coverage
• Voluntary Life Insurance & AD&D Coverage
• Employee Assistance Program (EAP)
• Company-paid Holidays
• Vacation
• Paid Sick Leave
• Telecommunication Monthly Stipend
• Work-From-Home Equipment Reimbursement

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