Regulatory Affairs Manager (Clinical Focus)

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!  

Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status. 

 Why you’ll love working at Axogen: 

• Friendly, open, and fun team culture that values unique perspectives 
• Company-wide dedication to profoundly impacting patients’ lives 
• Comprehensive, high-quality benefits package effective on date of hire 
• Educational assistance available for all employees 
• Matching 401(k) retirement plan 
• Paid holidays, including floating holidays, to be used at your discretion 
• Employee Stock Purchase Plan 
• Referral incentive program 

Axogen Mission and Business Purpose

Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.

Job Summary of the Regulatory Affairs Manager (Clinical Focus)

Reporting to the Sr. Manager, Regulatory Affairs, the manager will provide direction and leadership in the development and implementation of domestic and international regulatory strategies and processes for Axogen’s clinical programs in compliance with applicable regulations, recommended guidance, and standards. The manager will provide support to regulatory submissions, regulatory activities, cross-functional teams, and supervise the preparation of regulatory deliverables to support clinical programs in domestic and international markets. The manager is accountable for cross-functional alignment relating to clinical regulatory strategy and deliverables. The manager will review information related to safety for Axogen’s product portfolio and perform corresponding regulatory assessments. The manager will perform clinical-focused regulatory intelligence activities related to the markets in which clinical programs are being considered or are in effect. The manager will be responsible for the management of Regulatory Specialist(s) and Interns. The manager will assist in or direct interactions with regulatory bodies and participate in regulatory inspections.

Requirements of the Regulatory Affairs Manager (Clinical Focus)

• Bachelor’s degree required; in a scientific, regulatory, or health-related discipline preferred
• Minimum 4 years of experience in Regulatory Affairs, with at least 1 year focused on clinical programs.
• Demonstrated leadership experience (cross-functional team leadership).
• Experience in regulatory writing and submitting successful regulatory submissions in both domestic and international markets
• Prior experience in a regulated biologic, combination product, or device environment strongly preferred.
• Strong project management and strategic problem-solving skills; ability to manage multiple priorities in a fast-paced environment.
• Comprehensive knowledge relating to 21 CFR §210, 211, 312, 314, 600, 601, Current Good Clinical Practices (cGCPs), and ICH efficacy and safety guidelines.
• Ability to travel approximately 20% 

Responsibilities of the Regulatory Affairs Manager (Clinical Focus)

The specific duties of the Regulatory Affairs Manager (Clinical Focus) include but are not limited to:

• Acts as the Regulatory-Clinical representative on cross-functional clinical development teams to ensure regulatory requirements, recommended guidance and applicable standards are incorporated into the development process and continued compliance is maintained. 
• Provides regulatory oversight for assigned projects, focused on clinical development programs and the regulatory maintenance of active trials. 
• Participates in clinical risk-benefit analysis, providing input and a regulatory perspective regarding risk assessment. 
• Keeps Senior Management informed of the regulatory status of products’ clinical programs and significant regulatory issues and provides updates regarding new developments. 
• Leads and drives submission activities (planning, authoring, reviewi