Director, Regulatory Sciences

ProPharma•Washington, DC

About The Position

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Director, Regulatory Sciences will be responsible for leading and overseeing projects for US Regulatory science clients, managing a team of professionals, and ensuring the successful delivery of regulatory strategies, submissions, and other deliverables. Expertise in regulatory affairs, pharmaceutical industry knowledge, and leadership skills will be crucial in driving the organization's strategy and achieving business objectives.

Requirements

Strong leadership skills, with experience managing and developing high-performance teams.
Excellent written and verbal communication skills, with the ability to effectively interact with internal stakeholders, regulatory authorities, and external partners.
Strategic mindset, with the ability to analyze complex regulatory issues and provide innovative solutions.
Strong project management and organizational skills, with the ability to prioritize and manage multiple tasks simultaneously.
Bachelor's degree in a relevant scientific discipline, advance degree preferred.
A minimum of 7 years of experience in regulatory affairs within the pharmaceutical industry, with a focus on regulatory strategic and operational leadership knowledge.
In-depth knowledge of FDA regulations, guidelines, and requirements, including Hatch-Waxman Act and other relevant legislation.
Proven track record of successful regulatory submissions and approvals, with a through understanding of the regulatory processes and requirements.

Responsibilities

Develop and implement the overall strategy for regulatory submissions, approvals, and maintenance, aligned with the organization's goals and regulatory requirements.
Lead and mentor a team of regulatory professionals, providing guidance, support, and training to ensure high performance and professional development.
Stay updated on relevant regulations, guidelines, and industry trends, ensuring compliance and providing guidance to the team and stakeholders.
Oversee the preparation, review, and timely submission of high-quality client deliverables, including managing interactions with regulatory authorities.
Collaborate with cross-functional teams, including Research and Development, Manufacturing, Quality Assurance, and Legal, to ensure successful regulatory submissions within the defined timelines.
Ensure robust quality oversight for regulatory submissions, ensuring adherence to regulatory requirements and best practices.
Establish and maintain effective relationships with regulatory authorities, consultants, contract research organizations (CROs), and other external partners to support regulatory activities.
Provide input as requested into the department's budget, optimizing resource allocation and ensuring cost-effectiveness.
Identify and mitigate risks associated with deliverables and submissions, proactively addressing challenges and proposing solutions.
Other duties as assigned.