Senior Principal Scientist, US Regulatory Innovation

Dechra; United States; On-site; USD 140,000 - 190,000; Full time

Job summary

Dechra, an international veterinary pharmaceutical company, seeks a Regulatory Affairs Senior Principal Scientist to lead regulatory strategies for traditional small molecules and biologics in the US, shaping development paths and ensuring timely approvals.

The role mentors US team members, collaborates with FDA CVM/USDA CVB and cross-functional teams, and represents Dechra on external committees, with domestic/international travel ~10–20%.

Qualifications

• Extensive experience in animal health pharmaceutical regulatory affairs.
• Strong track record with US regulatory submissions and approvals.
• Experience collaborating with cross-functional teams and external regulators.
• Ability to mentor junior staff and lead RA projects.
• Demonstrated success navigating FDA CVM/USDA CVB processes.

Responsibilities

• Develop and implement risk-based regulatory strategies for drugs and biologics.
• Identify regulatory risks early and propose strategic options.
• Provide guidance to cross-functional teams on regulatory readiness.
• Represent US on project teams and align with global strategies.
• Prepare and review regulatory documents and submissions.

Skills

Regulatory affairs leadership

US FDA CVM/USDA CVB experience

Cross-functional collaboration

Regulatory submissions

Strategic regulatory planning

Education

BS/MS/PhD/DVM/VMD in life sciences

Job description

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%