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Associate Director, Regulatory Operations

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Rhythm Pharmaceuticals, Inc
Full Time position
Listed on 2026-01-29
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Salary/Wage Range or Industry Benchmark: 160000 - 240000 USD Yearly USD 160000.00 240000.00 YEAR
Job Description & How to Apply Below

Company Overview

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need.

Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

Opportunity Overview

The Associate Director (AD) of Regulatory Operations is responsible for assisting the Head of Regulatory Operations in maintaining Rhythm’s regulatory submission standards and current electronic submission guidelines/requirements. This role involves managing the preparation of eCTD submission-ready documents, coordinating across functions, and ensuring quality, accuracy, and adherence to regulatory guidelines. Additionally, the Associate Director supports the preparation and submission of Investigational New Drug applications (INDs), New Drug applications (NDAs), annual reports, Development Safety Update Reports (DSURs), and safety reports to regulatory authorities.

Responsibilities

and Duties
  • Manage regulatory operations activities, ensuring timely and accurate regulatory submissions, and collaborating with cross-functional teams for our US, EU, UK and Health Canada regions
  • Identify/address opportunities to enhance operational effectiveness and drive process improvements within the department
  • Manage regulatory operations activities, including preparation of eCTD submission-ready documents, coordination across functions, and adherence to regulatory guidelines and processes
  • Support development program projects by collaborating with multi-disciplinary project teams to ensure successful program deliverables
  • Assist in the development of Standard Operating Procedures (SOPs) quality assurance, and records management practices related to regulatory operations activities
  • Track regulatory department information such as commitments with health authorities and NDA/IND commitments
  • Act as an expert resource for eCTD submissions to FDA, ensuring compliance with internal and health authority standards
  • Support the development and maintenance of operations resources for submission documents
  • Identify new or revised regulatory policies and initiate activities to support compliance
  • Participate in special projects and process improvement initiatives
Qualifications and Skills
  • Bachelor’s degree in life/physical sciences or related field
  • 8+ years of highly relevant pharmaceutical/biotechnology experience in Regulatory Affairs Operations
  • Knowledge and understanding of the drug development process
  • Strong knowledge of FDA and Global EU/UK regulations and guidelines, especially CTD and eCTD structure
  • Experience with Veeva RIM EDMS
  • Highly proficient in Microsoft Office suite
  • Ability to balance both strategic and operational approaches, “think outside the box” and to manage multiple tasks in a fast-paced environment
  • Detail-oriented and highly organized
  • Excellent interpersonal skills and ability to develop collaborative partnerships with key stakeholders

This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involve travel.

The expected salary range for this position is $160,000 - $240,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.

More about Rhythm

We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated…

Position Requirements
10+ Years work experience
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