The Business Analyst will analyze business unit performance, generate insights, support forecasting, and collaborate with cross-functional teams to ensure operational excellence and data-driven decisions.

Lead regulatory strategies for drug development in Europe, manage teams, interface with regulatory agencies, and ensure compliance while mentoring staff.

The Associate Director leads the Central Monitoring team to ensure quality and timely delivery of clinical studies, develops staffing strategies, and mentors leadership talent.

The Data Product Manager leads data product strategies, facilitates stakeholder engagement, manages product roadmaps, and collaborates with cross-functional teams to enhance data solutions.

The SFE Manager leads customer segmentation, quarterly call planning, sales target setting, and manages the SFE team to optimize performance and develop skills, ensuring alignment with financial goals and enhancing data integrity.

Join AbbVie's Future Opportunities Talent Pipeline to express interest in future roles that align with your skills in healthcare advancements.

Coordinate the approval of promotional and non-promotional materials, ensuring compliance with regulations. Provide guidance on UK codes and support marketing campaigns.

The Medical Advisor provides strategic medical input for medical affairs, oversees clinical trials, and ensures compliance with regulatory requirements while educating stakeholders.

The Senior Manager of Regulatory Affairs oversees UK regulatory activities, leads a team, ensures compliance with regulations, and engages with health authorities to facilitate product approvals and launches.

The Medical Operations Lead role involves overseeing medical project execution, managing resources and teams, ensuring compliance, and enhancing operational efficiency within clinical research.

Responsible for implementing registration strategy for regulatory approval of pharma products in Europe, ensuring compliance and lifecycle management, and coordinating regulatory activities.

The role entails leading the Dermatology sales and marketing teams, managing brand performance and P&L, and collaborating cross-functionally to achieve growth while driving strategic initiatives within the Immunology Business Unit.

The Senior Project Manager will manage regulatory affairs for oncology in the UK, oversee submission processes, ensure compliance with regulations, and lead strategic initiatives for product lifecycle management.

AbbVie is looking for experienced Medical Affairs leaders for their Future Leaders Talent Pipeline, focusing on evidence-based medicine and therapeutic innovation. Candidates should have a strong scientific background and leadership experience in areas like immunology, oncology, or neuroscience to contribute to impactful clinical outcomes.

The Country Clinical Operations Head oversees clinical operations in the country, ensuring trials are managed efficiently and meet quality standards. Responsibilities include strategic planning, team leadership, and resource management, while ensuring compliance with regulations and promoting continuous improvement.

Responsible for regulatory approval and lifecycle management of pharmaceutical products in Europe, ensuring compliance and supporting global strategies.

The Employee Relations Manager oversees employee relations, manages grievances, advises on labor law, resolves conflicts, and develops strategies for employee engagement.

The TA Director leads risk management strategies across clinical development portfolios, develops teams, and ensures quality oversight for therapeutic areas.

The Senior Brand Manager will lead strategic planning for the lymphoma portfolio, support launches, execute multichannel campaigns, and manage cross-functional stakeholder partnerships, all in compliance with the ABPI Code.