Senior Director, Regulatory Affairs

Clinical Dynamix, Inc.; Jersey City (NJ); Hybrid; USD 210,000 - 320,000; Full time

Job summary

Clinical Dynamix, Inc. in New Jersey seeks a Senior Director, Regulatory Affairs to lead global regulatory strategy, guide FDA submissions and lifecycle management for medical products.

Hybrid work arrangement in Northern NJ is available. The ideal candidate has 15+ years in regulatory affairs, an advanced life sciences degree, and a proven capability to direct policy, regulatory intelligence, and cross-functional collaboration with external partners.

Qualifications

• 15+ years of progressive experience in regulatory affairs with global scope.
• Mastery of global regulatory agencies, processes and regulations.
• Proven record of medical product filings (INDs, NDAs, BLAs, MAAs).
• Excellent writing and verbal communication; ability to influence stakeholders.

Responsibilities

• Secure US and global regulatory marketing authorization for new products and updates.
• Lead preparation, review and submission of regulatory documents to FDA and regulators.
• Develop and implement policies, processes and SOPs for regulatory affairs.
• Formulate regulatory strategies for pipeline products and lifecycle management.
• Monitor regulatory updates and provide training on requirements.
• Maintain licenses, registrations and listings; act as SME on regulatory matters.
• Represent company in external meetings with regulators and development partners.

Skills

Regulatory leadership

Global regulatory knowledge

Regulatory submissions

Effective communication

Education

PharmD/PhD/MD/MA in Life Sciences

Job description

Senior Director, Regulatory Affairs - Northern NJ (Hybrid)

Client is seeking a capable, insightful, experienced Senior Director, Regulatory Affairs

Position Summary:

The Senior Director, Regulatory Affairs is responsible for providing subject matter expertise on matters related to global regulatory activities, as well as providing leadership for the growth and responsibilities of the regulatory department. The Senior Director will represent Company in key stakeholder and strategy meetings on regulatory matters related to medical product development and commercialization, including meetings with executive leadership, meetings with the Food and Drug Administration (FDA) and other regulators. This role leads preparation, review, and submission of documents to the FDA and other regulatory authorities to support product development leading to marketing authorization and lifecycle management. This role combines scientific, regulatory, and business knowledge to assure that Company products are developed and distributed according to all applicable regulations in alignment with the company’s strategic goals. The role requires a mastery of medical product regulations to develop efficient solutions to the evolving regulatory needs of the industry.

Responsibilities:

• Secure US and global regulatory marketing authorization for new products, product updates, and product expansions. This includes preparation and filing of submissions, responding to regulatory authorities and auditors, and leading meetings with regulatory authorities.
• Develop and implement a comprehensive set of policies, processes, and SOPs in support of the organization’s regulatory responsibility.
• Formulate regulatory strategies for pipeline products.
• Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop strategies for resolution.
• Perform global regulatory intelligence including monitoring regulatory updates, workshops, discussions, and other news sources.
• Advance internal awareness of current and upcoming regulations, requirements, and expectations, and identify training and educational needs for the organization.
• Manage processes involved with maintaining annual licenses, registrations, and listings.
• Serve as an internal go-to subject matter expert on regulatory and quality matters.
• Represent the company in external meetings on regulatory matters, including with regulators and auditors and development partners.

Requirements and Preferred Skills:

• Advanced degree in Life Sciences required (PharmD, PhD, MD, MA)
• 15+ years of progressive experience in regulatory affairs, with increasing scope of responsibility and demonstrated leadership at the global level
• Knowledge of global regulatory agencies/processes/regulations
• Record of successful medical product filings such as INDs, NDAs, BLAs, MAAs
• Excellent writing and oral communication skills, with the ability to convey complex scientific and regulatory concepts clearly and persuasively
• Ability to form and maintain working professional relationships with external stakeholders, regulatory authorities and scientific and clinical advisors
• Prior experience and demonstrated ability to work in diverse therapeutic areas
• Strong leadership skills with ability to set a vision, lead change, grow a team and mentor others
• Experience leading regulatory authority communications and meetings