Senior Principal Scientist, US Regulatory Innovation

Dechra; Boston (MA); On-site; USD 150,000 - 220,000; Full time

Job summary

Dechra, a leading veterinary pharmaceutical company, seeks a Regulatory Affairs Senior Principal Scientist to lead regulatory strategies for traditional small‑molecule drugs and biologics in the US. You will identify risks and opportunities, mentor junior staff, and collaborate with FDA CVM/USDA CVB to align development pathways and labeling.

You will shape regulatory submissions, provide cross‑functional guidance, and represent US RA on global teams, ensuring timely product development and

Qualifications

• University degree (BS, MS, PhD, DVM/VMD) in veterinary medicine, animal sciences, or a related life science discipline.
• Extensive experience in animal health pharmaceutical regulatory affairs, including supporting product development, with some experience focused on safety and efficacy.
• Proven experience leading regulatory submissions for small and large‑molecule biopharmaceutical products in the US.
• Demonstrated success obtaining approvals or advancing drug and biopharmaceutical products through FDA CVM/USDA CVB submissions.
• Strong understanding of US clinical and safety requirements for drug and biopharmaceutical products.
• Experience interacting directly with regulatory authorities.

Responsibilities

• Develop, lead, and deliver regulatory strategies for drugs and biotherapeutics in the US.
• Identify regulatory risks and opportunities early and develop strategic options.
• Provide scientific and regulatory guidance to cross‑functional teams, supporting regulatory readiness.
• Represent the US region on cross‑functional drug and biotherapeutic development teams.
• Prepare, review, or oversee regulatory documents, including pre‑submission conference requests and protocol concurrences.
• Work with FDA CVM/USDA CVB to discuss development pathways and labeling text.
• Stay up to date with changing US and global regulations and share insights with senior stakeholders.
• Represent Dechra on external committees and regulatory policy discussions.
• Provide senior‑level scientific and regulatory leadership to Clinical, CMC, Safety and Biotherapeutics teams.
• Serve as Global RA representative when assigned.

Skills

Regulatory affairs

US FDA CVM/USDA CVB knowledge

Biotherapeutics regulatory experience

Strategic regulatory planning

Cross-functional leadership

Education

DVM/VMD preferred

BS/MS/PhD in life sciences

Job description

Welcome to Dechra

Dechra is an international veterinary pharmaceutical business focused on specialty products. We develop, manufacture, sell and market high-quality products exclusively for veterinarians around the world.

Job Purpose

The Regulatory Affairs Senior Principal Scientist leads and delivers thoughtful, forward‑looking regulatory strategies for the clinical safety and efficacy of traditional small‑molecule drugs and large‑molecule biotherapeutics, including monoclonal antibodies and other complex biologics, in the US.

This role identifies regulatory opportunities and risks early, develops strategic options and helps ensure regulatory pathways support successful and timely product development across all US programs.

The role may also represent Global RA on project teams and work with regional RA teams to support a global registration strategy. In addition, the Senior Principal Scientist mentors junior members of the US Innovation Regulatory Affairs team, helping them build technical regulatory skills in clinical safety and efficacy.

Key Responsibilities

• Develop, lead, and deliver innovative, risk‑based regulatory strategies for drugs and biotherapeutics (e.g., monoclonal antibodies, protein therapeutics).
• Identify regulatory risks and opportunities early and develop strategic options to address or make the most of them throughout the development lifecycle.
• Provide scientific and regulatory guidance to cross‑functional project teams, supporting strategic decisions, regulatory readiness and continued development of regulatory expertise.
• Represent the US region on cross‑functional drug and biotherapeutic development teams and help ensure alignment with US regulatory expectations.
• Prepare, review, or oversee regulatory documents, including pre‑submission conference requests, protocol concurrences, and Effectiveness and Target Animal Safety technical sections, helping the US Innovation RA team maintain consistent, high standards.
• Work directly with FDA CVM/USDA CVB to discuss and agree on development pathways, protocol concurrence, labeling text and product approval.
• Keep up to date with changing US and global drug and biotherapeutic legislation and share clear, strategic insights with senior stakeholders.
• Represent Dechra on relevant external committees, working groups and trade associations for drugs and biotherapeutics, contributing to agency guidance and regulatory policy.
• Provide senior‑level scientific and regulatory leadership to Clinical, CMC, Safety and DRD/Biotherapeutics Development teams.
• Serve as Global RA representative when assigned, helping ensure alignment with EU, US, and international SMEs.

Skills & Experience

• University degree (BS, MS, PhD, DVM/VMD) in veterinary medicine, animal sciences, or a related life science discipline.
• DVM/VMD is preferred. Candidates with other backgrounds (BS, MS, PhD) may also be considered if they have relevant animal health experience.
• Extensive experience in animal health pharmaceutical regulatory affairs, including supporting product development, with some experience focused on safety and efficacy.
• Demonstrated proficiency and hands‑on experience with regulatory submissions and approvals, from new product development through commercialization.
• Proven experience leading regulatory submissions for small and large‑molecule biopharmaceutical products in the US.
• Demonstrated success obtaining approvals or advancing drug and biopharmaceutical products through FDA CVM/USDA CVB submissions.
• Strong understanding of US clinical and safety requirements for drug and biopharmaceutical products.
• Experience interacting directly with regulatory authorities.
• Proven success in achieving objectives comparable to those of this position.

Ability to travel (domestic/international) approximately 10-20%.