Jobs at AbbVie

Serve as a Medical Science Liaison for AbbVie’s rheumatology team across South England. Build relationships with healthcare experts, lead scientific discussions and educational presentations, support clinical research and real-world evidence activities, gather field insights, and represent AbbVie at scientific meetings. Collaborate with Medical Affairs, Clinical Operations, and Commercial teams to improve patient outcomes. The field-based role requires 75% travel and a full UK driving licence.

Reviews and approves UK and overseas pharmaceutical meetings and non-promotional materials for ABPI, MHRA, EFPIA, IFPMA, and national code compliance. Advises medical and commercial teams, evaluates risk, supports corrective actions, presents compliance cases, and serves as the subject matter expert for meeting approvals and materials review.

Leads and manages Central Monitoring Managers responsible for de-risking clinical studies through risk-based quality management and central monitoring. Oversees staffing strategy, service delivery, recruitment, training, performance management, coaching, and leadership development. Partners with cross-functional Clinical Development Operations stakeholders to ensure high-quality, efficient, timely study execution. Promotes risk-based quality management, data-driven decision-making, continuous improvement, and effective issue resolution across global and remote teams.

Leads clinical study start-up and maintenance activities across assigned countries and sites, ensuring timely, compliant, and high-quality activation. Coordinates regulatory, ethics, contracts, clinical supplies, essential documents, ICF approvals, site activation, metrics, and inspection readiness. Acts as a subject matter expert, mentors junior specialists, supports process improvements, and drives adoption of new technologies and workflows.

Leads study-level clinical site management strategy and deliverables from planning through closeout. Oversees site selection, activation, engagement, monitoring, protocol adherence, data cleaning, database locks, closure, compliance, risk mitigation, TMF completeness, and inspection readiness. Coordinates SMLs, country teams, and clinical study stakeholders while managing timelines, resources, quality, and issue escalation across global clinical trials.

Coordinates patient advocacy group meetings and patient engagements, including logistics, agendas, briefing materials, records, action tracking, and follow-up. Provides project and administrative support across therapy areas, collaborates with internal stakeholders, and helps ensure compliant delivery under AbbVie policies and the ABPI Code of Practice. Maintains accurate relationship and commitment documentation while escalating risks and supporting Government Affairs and Patient Advocacy Managers.

Leads proactive, end-to-end talent acquisition for critical and niche roles. Partners with hiring managers and business leaders, develops sourcing and talent attraction strategies, uses market intelligence and recruitment analytics to guide workforce planning, builds diverse talent pipelines, improves candidate experience and recruitment processes, and supports long-term organizational growth and inclusive hiring.

Leads and develops clinical research teams, including CRA hiring, mentoring, performance management, resource allocation, and monitoring oversight. Ensures clinical studies meet timelines, budgets, quality standards, GCP, ICH, and regulatory requirements. Supports audit readiness, CAPA implementation, risk mitigation, KPI achievement, stakeholder engagement, and process improvement across therapeutic areas and study phases.

Develop and execute integrated internal and external communications for AbbVie UK across corporate, therapy area, digital, social, media, intranet, and leadership channels. Create and edit content, support issues communications, advise stakeholders, manage agencies and vendors, measure performance, and ensure activity meets governance, compliance, budget, and quality standards in a regulated pharmaceutical environment.

Leads global and area-level clinical site management activities across assigned studies, ensuring site monitoring strategy, engagement, activation, compliance, timelines, data-cleaning milestones, database locks, and site closeout. Manages risks, supports inspection readiness, drives Trial Master File completeness, coordinates resources, and influences cross-functional stakeholders in a matrix environment. The role requires strong clinical research, monitoring or project management experience, planning, communication, leadership, and Microsoft Office skills.

Act as the named final signatory for UK and Ireland, certifying promotional and non-promotional materials meet ABPI/IPHA/MHRA/HPRA codes. Provide brand support, give compliant solutions, review and approve materials, advise affiliates, participate in review projects, and present code cases to stakeholders.

Leads international real-world evidence strategy and execution across affiliates, therapeutic areas, and cross-functional teams. Serves as an RWE subject matter expert, translates evidence gaps into study designs, coordinates RWD expertise, supports integrated evidence planning, develops RWE networks, and contributes to area and asset evidence teams. The role also monitors RWE innovations and guidelines, engages vendors and external stakeholders, provides training, and represents AbbVie in RWE workstreams and consortia.

Leads UK regulatory affairs for a neuroscience therapeutic area, overseeing regulatory strategies, submissions, licensing, compliance, audits, inspections, product launches, and interactions with MHRA and industry associations. Manages a small regulatory team, develops talent, advises cross-functional stakeholders, monitors regulatory intelligence, and ensures alignment between UK and global strategies.

Leads international regulatory strategy for pharmaceutical advertising and promotion. Advises Commercial, Medical, Legal, Compliance, affiliates, and external stakeholders on regulations and industry codes. Reviews promotional materials and campaigns, manages risk strategies, supports brand initiatives, and provides regulatory guidance throughout asset development. Leads team operations, initiatives, and improvement plans while balancing business objectives, innovation, and compliance.

Designs, deploys, and maintains predictive and prescriptive models and advanced analytics solutions for business needs. Partners with stakeholders to translate commercial problems into analytical frameworks, move solutions into production, and ensure compliance, governance, and measurable business impact. Communicates model outputs and recommendations to technical and non-technical audiences while collaborating cross-functionally across business, analytics, and technical teams.

Lead and manage employee relations in the UK: investigations, grievances, disciplinaries, mediation, policy development, legal compliance, stakeholder partnership, ER training, metrics analysis, and resolution recommendations.

Lead the Oncology commercial organization to define and execute local brand strategy, launch plans and P&L accountability. Manage and develop sales and marketing teams, align cross-functional stakeholders (Medical, Market Access, Regulatory), optimize resources, drive sales performance and ensure launch readiness for pipeline assets.

Manage and grow dermatology accounts in North Scotland by executing in-field brand strategy, building HCP relationships, driving sales through targeted engagement, developing territory business plans, sharing market intelligence, and collaborating with medical and market access colleagues. Ensure compliance and ABPI standards.

Field-based pharmaceutical sales role responsible for executing in-field dermatology brand strategy, building HCP relationships, driving territory sales, gathering market intelligence, and collaborating with medical and market access colleagues. Requires ABPI qualification, proven pharma sales success, territory planning, NHS navigation, and adherence to compliance.

Lead Regulatory data standards and governance, implement enterprise data governance, map and harmonize regulatory data across systems, act as ISO IDMP SME, represent AbbVie in industry forums, support COSMOS RIM and ontology initiatives, and drive tools, training, and process improvements for regulatory data interoperability and compliance.