Associate Director, Regulatory Liaison (Immunology & Pulmonary Hypertension) (m/f/x, 100%)

Janssen Biologics, a member of Johnson & Johnson’s Family of Companies, is recruiting for a Associate Director, EMEA Regulatory Liaison in Immunology & Pulmonary Hypertension.

The preferred position location is Leiden, Netherlands. Other additional locations are High Wycombe, UK; Beerse, Belgium and Zug, Switzerland.

Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit www.JanssenRnD.com for more information and join us!

Our company thrives on a diverse company culture, celebrating the uniqueness of our employees and is committed to inclusion. Janssen is proud to be equal opportunity employer. Our culture is interconnected by the shared values of Our Credo. It is a culture that celebrates diversity and diverse perspectives, and helps its employees achieve an effective balance between work and home life and supports their efforts to have a positive impact on their communities.

Main Responsibilities:

Strategic and tactical input in development, post-approval and Life cycle management

• Advise the Project Team and/or Regional Therapeutic Area Leader on applicable regulatory issues, project-specific regulatory issues, and issues related to regional regulatory climates
• Drive understanding of central and national regulatory requirements
• Develop and ensure effective implementation of regional (central and national) regulatory strategy and tactics in support of the global development and life-cycle management plan
• Develop a deep understanding of the regional regulatory environment, competitor intelligence and therapeutic area
• Provide input for developing and updating the Target EU SmPC based on an understanding of the implications of regional regulatory strategy for labeling
• Ensure appropriate implementation of scientific advice / Regulatory Agency comments into development and life-cycle management plan

Liaison with Regulatory Agencies and Local Operating Companies

• Establish and maintain positive relationships with Regulatory Agencies and effectively negotiate with Regulatory Agencies on product-specific labeling, study design, submissions content, and post-approval commitments
• Act as primary contact with EMEA. Work through LOC and/or CRO for National Regulatory Agencies contacts, as appropriate
• Ensure appropriate involvement and liaise with LOC regulatory affairs personnel to facilitate local Regulatory Agency meetings
• Determine timing and strategy for Regulatory Agency meetings and scientific advice
• Prepare team, lead, conduct and facilitate contacts/meetings with Regulatory Agencies. Define attendance in consultation with GRL and CDT. Issue minutes and contact reports and disseminate correspondence, faxes, contact reports from contacts with Regulatory Agencies
• Ensure that issues raised by Regulatory Agencies are promptly and adequately addressed
• Negotiate labeling with Regulatory Agencies, going through each of the back-up strategies if necessary

Input in document and process development

• Advise team on required documents and processes to support Regulatory Agency contacts and submission
• Plan and develop briefing documents for meetings with Regulatory Agencies, including determining content and review of documents
• Provide input to and review submission documents to ensure that they are fit for purpose and support labeling statements as appropriate
• Define, generate and submit appropriate data-driven (regional/local) responses to Regulatory Agency questions
• Ensure necessary regulatory activities are planned and adequately tracked in company systems

Clinical Trial Applications (CTA)

• Ensure protocols are developed in alignment with regional registration strategies to support registration, reimbursement and competitive labeling
• Advise team on required documents and submission strategies in preparation of CTA
• Ensure CTA submission packages are complete and available according to agreed timelines

Marketing Authorization Application (MAA)

• Provide regulatory support throughout registration process and life-cycle management
• Manage submissions, define submission plans, and advise team on required documents and submission strategies in preparation of MAAs (in collaboration with LOCs as appropriate)
• Ensure timely MAA availability, track critical path activities
• Responsible for submission and acceptance of MAA
• Ensure country-specific submission packages are made available to the LOCs

Resource Planning and Management

• Determine resource requirements for assigned projects and anticipate needs for major filings
• Provide line management, coaching and guidance to Regulatory Professionals as appropriate

Qualifications

Education and experience

• University degree - medical or paramedical (pharmacy, biology, veterinary etc.) required
• Breadth of regulatory experience in drug development and commercialization (e.g. experience in multiple products, multiple phases of development, multiple therapeutic areas)
• Experience with EU regulatory procedures (CP, MRP, national) essential
• Experience in working in project teams and/or a matrix organization required
• Previous Immunology experience preferred

Skills

• Negotiating and conflict handling
• People management
• Complex project management
• Oral & written communication
• Organization & multi-tasking

Knowledge

• Excellent knowledge of English
• Knowledge of the applicable therapeutic area
• In depth knowledge of the regulatory environment, guidelines, and practice of EMEA regions

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location
Netherlands-South Holland-Leiden- Other Locations
Europe/Middle East/Africa-Belgium-Antwerp-Beerse, Europe/Middle East/Africa-United Kingdom-England-High Wycombe, Europe/Middle East/Africa-Switzerland
Organization
Janssen Biologics (7266)
Job Function
Regulatory Affairs
Requisition ID
2105977221W