- Lead and manage the team responsible for aligning local medical/regulatory services with the global strategy.
- Act as a reviewer and signatory as needed.
- Provide support and training on the ABPI Code of Practice.
- Act as a project manager for Development Consulting & Scientific Affairs projects.
- Recruit and onboard team members with the right skills.
- Offer guidance and mentorship to aspiring signatories.
- Deliver ABPI training, audits, SOP development, and consultancy support to clients.
- Be the key point of contact for commercial and operational matters with the global practice area.
- Manage and develop processes and tools for PMC services in the UK/IE.
- Collaborate with various stakeholders for proposal responses and quotes.
- Participate in local and global meetings to represent medical requirements.
- Ensure high-level utilization and capability oversight of trained personnel.
- Drive team utilization in line with global KPIs.
- Maintain vendor relations and ensure compliance.
- Monitor issues/lessons learned for service improvement.
- UK-registered pharmacist preferred.
- Experience in the pharmaceutical industry and consulting.
- Strong knowledge of regulatory frameworks including ABPI, IPHA, and EFPIA Codes of Practice.
- Familiarity with MHRA and HPRA roles in promotional material oversight.
- Well-connected in the UK/IE pharmaceutical field.
- Ability to lead, collaborate, and work independently.
- Strong interpersonal and problem-solving skills.
- Business acumen and ability to offer solutions pragmatically.
- Flexibility, adaptability, and structured approach to work.
- Proactive in identifying cross-selling opportunities.
- Excellent communication and presentation skills.
- 25 days holiday plus BH.
- 8% employer pension contribution.
- Positive work/life balance environment.
- Continual development opportunities through training and experience.
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