Sr. Manager/Associate Director, Regulatory Writer

Job Description

Job Description

Position: Regulatory Writer (Sr. Manager/Associate Director)
Department: Development – Regulatory Affairs
Location: Remote (PST Zone) with occasional travel for team and client meetings
Reports To:  Executive Director, Global Regulatory Affairs

P osition Summary
The Senior Manager/Associate Director, Regulatory Writing will serve as the lead regulatory writing professional across Angitia's development portfolio and will be responsible for planning, authoring, coordinating, and delivering high-quality regulatory documents supporting global development programs from IND through marketing application and lifecycle management activities. This individual will provide strategic document leadership, working closely with Regulatory Affairs, Clinical Development, Biometrics, Safety, Nonclinical, CMC, and external partners to develop clear, scientifically rigorous, and submission-ready documentation. The role will establish document standards and best practices, manage document timelines, and ensure consistent, inspection-ready content across all regulatory deliverables. The successful candidate will function as a key member of cross-functional development teams and serve as the primary writing lead for major regulatory submissions and health authority interactions.

R e sponsibilities

• 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.

Q ualifications

• 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.

Preferred

• 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.

Salary Range: $140K to 170K

About Angitia
Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 2 biologic product candidates in the clinic for the treatment of osteoporosis, and osteogenesis imperfecta (OI). Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built its headquarters in Westlake Village, CA, USA, and offices in Guangzhou, China, which is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. The company is committed to serving patients in need by carrying out innovative science, including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group. 

Learn more at  

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