Jobs and Careers

Associate Director, Regulatory Affairs - Combination Products

Morrisville, United Statesfull_timeVerifiedPosted 5 Nov 2024

About the role

Is Kymanox the right fit for you?        You want to make a difference and have an impact…      You enjoy having an influence in your day-to-day work…      You are motivated by working alongside a team filled with                   subject matter experts who will help you learn and grow…      You wake up every day and do what you do             … because patients deserve better.   If this sounds like you, you’ve come to the right place. The Associate Director, Regulatory Affairs will join our team and play a key role in providing both technical and managerial leadership to principal, senior, and associate level resources through both direct and indirect reporting structure. This role will also be responsible for leading regulatory service projects by providing robust regulatory strategies, leading interactions with regulatory agencies, and preparing regulatory applications for drug products, biologics, medical devices, and combination products. This position involves high-level strategic planning as well as tactical responsibilities. Services may be provided at a client site, from a Kymanox office, or remotely. Responsibilities:

Provide leadership to external-facing Kymanox project teams with accountability for project strategy, execution, success, and client satisfaction.

Lead planning and execution of regulatory activities. Delegate and monitor quality and progress of work, providing technical support and direction to project teams.

Lead and attend meetings with regulatory authorities. Serve as the Regulatory Point of Contact to regulatory authorities, as requested by clients.

Prepare regulatory applications, including expedited pathway programs, for regulatory authorities on behalf of Kymanox clients.

Review and edit dossiers, briefing books, and responses to regulatory authority questions; work with experts and authors to prepare information for regulatory applications and ensure submission readiness.

Perform technical and regulatory review of source documents.

Manage regulatory application timelines in accordance with client expectations and regulatory authority requirements. Inform clients of regulatory risks.

Work directly with eCTD publishing resources to ensure accurate linking; complete necessary forms required for application submissions.

Manage application communication logs with regulatory authorities for client programs.

Perform due diligence reviews and inform executive counsel/investors of regulatory risks, as requested by clients.

Provide mentorship and development opportunities to regulatory team, as part of cross-functional projects or as direct reports.

Provide functional management and leadership of direct reports within team.

Responsible for team performance reviews and evaluations, mentoring and coaching, resource management, goal setting, and time tracking and reporting.

Support internal business initiatives to improve Kymanox processes and practices. Evaluate future business needs and derive/implement strategies to meet those needs