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Associate Director, Regulatory Affairs Operations

Alkermes
Full-time
On-site
Waltham, Middlesex, United States
$153,000 - $171,000 USD yearly
Description

The Associate Director, Regulatory Operations will be responsible for submission management across the development pipeline and support the commercial portfolio. This hands-on position will also assist with regulatory affairs systems, applications, and tools including supporting system implementations, maintenance, updates, and releases.

You’ll work closely with Regulatory Affairs and cross-functional partners to manage timelines, ensure submission readiness, and strengthen operational excellence across the organization.

Key Responsibilities: 

  • Lead end-to-end management of regulatory submissions, ensuring timely, compliant, and high-quality deliverables.
  • This role interfaces with external publishing vendor(s) for the preparation of submissions, and internal stakeholders to provide operational oversight and support for eCTD regulatory submission activities.
  • Serve as submission manager and primary contact for publishing vendors and internal stakeholders.
  • Oversee regulatory document management, tracking, and archival activities.
  • Manage regulatory systems (e.g., Veeva RIM, PromoMats), and serve as internal subject matter expert (SME) for training and support to internal stakeholders
  • Develop and implement processes, templates, and tools that improve submission efficiency and consistency.
  • Partnering with IT to maintain the regulatory technology landscape including maintenance, updates, and releases. 
  • Provide subject matter expertise on regulatory technologies and submission best practices.
  • Monitor new regulations and industry trends to assess impact on operational practices.

 

Basic Qualifications: 

  • Bachelor’s degree in a scientific or related field.
  • At least 10 years of related experience, with at least 8 years of regulatory operations experience in the biotech or pharmaceutical industry.

Preferred Qualifications: 

  • Strong understanding of eCTD submission standards and regulatory requirements across global regions.
  • Proven experience with IND/CTA and NDA/MAA submissions, including lifecycle management.
  • Hands-on experience with Veeva RIM and/or PromoMats strongly preferred.
  • Experience managing outsourced publishing vendors a plus.
  • Skilled at balancing strategic oversight with hands-on execution.
  • Strong communicator and collaborator with excellent organizational skills.

 

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Qualifications

The annual base salary for this position ranges from $153,000 to $171,000. In addition, this position is eligible for an annual performance pay bonus.  Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package.  Additional details can be found on our careers website: www.alkermes.com/careers#working-here  



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