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A global healthcare leader seeks an Associate Director in Barcelona to oversee global governance for Managed Access Programs (MAPs) and Post-Study Drug Supplies (PSDS). This pivotal role requires extensive experience in the pharmaceutical industry, with strong governance knowledge and leadership skills. You will collaborate cross-functionally to ensure compliance and quality in medicines reaching patients.
Step into a high-impact role where your expertise will shape global standards for Managed Access Programs (MAPs) and Post-Study Drug Supplies (PSDS). As Associate Director, you’ll drive enterprise-wide governance, ensuring quality, compliance, and patient-centricity across Novartis. Collaborating with senior leaders and cross-functional teams, you’ll influence strategic decisions, mitigate risks, and champion continuous improvement. This is your opportunity to make a meaningful difference in how medicines reach patients, while fostering a culture of integrity, innovation, and excellence.
Location: Barcelona, Spain. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Define global standards and develop policies, procedures, systems, and tools for MAPs and PSDS in line with regulations
Ensure consistent implementation of governance standards across country organisations and global functions
Lead enterprise-wide oversight for assigned processes, products, and services to ensure compliance and quality
Drive continuous improvement initiatives and cross-functional projects to simplify and enhance governance practices
Deliver training and learning opportunities to promote adherence and foster a collaborative, quality-focused culture
Identify and mitigate quality and compliance risks in collaboration with Legal, Ethics, Risk & Compliance, and Patient Safety
Promote change management and patient-centricity by aligning global and local governance efforts
Establish internal controls and support audits, country exchanges, and self-assessments to monitor compliance
Communicate effectively with senior leaders and present governance updates to global and local management boards
Support corrective actions and global audit readiness to ensure inspection success and regulatory alignment
Master’s degree in a scientific discipline
8+ years of experience in clinical, public health, or pharmaceutical industry roles
Strong governance knowledge across medical affairs, drug development, patient safety, and compliance
Proven leadership in global matrix teams and cross-functional project delivery
Skilled in influencing senior stakeholders and facilitating strategic decisions
High learning agility and commitment to continuous improvement
Excellent communication across diverse audiences and organisational levels
Strong relationship-building skills with internal and external stakeholders
Experience supporting global audits and inspections within a pharmaceutical or healthcare setting
Familiarity with change management strategies to embed quality and compliance culture
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Agility, Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care, People Management, Pharmaceutics, Priority Disease Areas Expertise, Product Launches, Product Strategy, Real World Evidence (RWE), Regulatory Compliance, Research Methodologies {+ 3 more}