Associate Director/Director of Regulatory Affairs (Boston) Job at RBW Consulting LLP, Boston, MA

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  • RBW Consulting LLP
  • Boston, MA

Job Description

I'm currently partnered with an oncology biotech who is looking to add an experienced Associate Director or Director of Regulatory Affairs to their team.

This is a fantastic opportunity to work within a one-of-a-kind organization with a fantastic culture, significant amount of funding, and assets in both early and late stage. The team has progressed their pipeline significantly over the past several years.

Key Responsibilities:

  • Develop and implement global regulatory strategies to support clinical and commercial goals.

  • Lead the preparation and maintenance of regulatory submissions (e.g., IND/CTA, NDA/MAA).

  • Draft regulatory documentation and respond to agency questions in collaboration with regulatory operations.

  • Lead communications with global health authorities, including preparation of briefing packages, meetings, and follow-up documentation.

  • Guide cross-functional teams on regulatory requirements and expedited pathways.

  • Assess regulatory risks and provide mitigation strategies to leadership and project teams.

  • Ensure full compliance with applicable regulations and internal policies.

  • Contribute regulatory insight into development plans, labeling, and post-approval activities.

  • Stay informed on evolving regulations and communicate key developments to stakeholders.

Qualifications:

  • Bachelor's degree in Life Sciences; advanced degree (PharmD, MS) preferred.

  • 5+ years of biotech/pharma industry experience in regulatory affairs.

  • Proven success in IND/CTA planning and execution, NDA/post-approval regulatory activities, and drug labeling.

  • Exceptional written, verbal, and organizational skills.

  • Demonstrated ability to think critically, influence cross-functional teams, and operate with integrity and patient-centered decision-making.

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Job Tags

Full time,

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