LAR-2411-365REGULATORY AFFAIRS ASSOCIATE DIRECTORMADRIDRegulatory Affairs Associate Director Opportunity – Join a Leading Pharmaceutical Company in Madrid, Spain!At MCR International, we're thrilled to announce an exclusive opportunity for a Regulatory Affairs Associate Director with a renowned global pharmaceutical company.
This strategic role, based in Madrid, Spain, offers a unique chance to shape and implement groundbreaking regulatory strategies on a global scale, directly aligning with the company's overall business objectives.Role Overview:As the Regulatory Affairs Associate Director, your primary mission will be to develop and execute innovative global regulatory strategies that drive product development and approval across international markets.
This role requires a deep understanding of complex regulatory landscapes and the ability to collaborate effectively with major Health Authorities (US, EU, Japan, and China) to ensure successful compliance and approval.Key Responsibilities:Strategic Leadership: Spearhead the development and execution of integrated global regulatory strategies for assigned projects and products.Global Representation:Act as the company's regulatory representative in communications with regulatory authorities, contractors, and corporate partners.Clinical & Pre-Clinical Guidance: Oversee regulatory strategies related to clinical and pre-clinical product phases, supporting lifecycle management and clinical development planning.Risk Mitigation: Assess and mitigate regulatory risks, providing crucial guidance to internal teams throughout the R&D process.Submission Oversight: Lead global regulatory submission processes, including marketing applications, briefing packages, and CTA submission strategies.Cross-Functional Collaboration: Advise and collaborate with cross-functional teams on global regulatory requirements, ensuring alignment with strategic objectives.Regulatory Insights: Monitor and analyze regulatory agency activities, assess their impact on ongoing programs, and provide timely strategic advice.Mentorship & Development:Mentor and guide Regulatory Project Managers and foster their development within the organization.What We're Looking For:Qualifications:- Degree in Life Sciences or a related field is required; an advanced degree (PharmD, MSc, PhD, MBA) is preferred.Experience:Industry Expertise:Minimum of 8 years in the pharmaceutical or biotechnology industry, with at least 6 years in Regulatory Affairs (Strategy).Global Regulatory Knowledge: In-depth understanding of regulatory landscapes in the US, EU, and Japan, with direct experience engaging with regulatory bodies such as FDA, EMA, and PMDA.Submission Experience: Proven track record of preparing and managing major regulatory submissions and amendments.Cross-Cultural Sensitivity: Experience in multinational settings and leading multidisciplinary teams.Key Skills:Leadership & Communication: Exceptional leadership abilities, with strong interpersonal skills for effective collaboration across senior management, scientific, and manufacturing teams.Organizational Excellence: Strong organizational skills to prioritize workloads effectively in a dynamic environment.Strategic Vision:Ability to set direction, influence decision-making, and represent the company in high-stakes regulatory discussions.If you're ready to take on a pivotal role that will shape the future of global regulatory strategy within a highly respected pharmaceutical organization, we invite you to apply.
This is an extraordinary opportunity to lead, innovate, and make a lasting impact on the global healthcare landscape.#J-18808-Ljbffr