About the job
12 month contract | Ireland, primarily remote with flexibility to travel to South Dublin
Role OverviewMorgan McKinley is partnering with a top-tier global biotechnology company to support their international external supply operations.
Serving as a key finance partner to the External Supply team, this role oversees all pre-commercial clinical and development program spend (P&L Net Expense). You will provide financial guidance, spend management, and reporting insights across a complex network of CDMOs and suppliers. The position reports directly to the Finance Director of External Supply, Operations Finance.
- Key ResponsibilitiesProgram Spend Management: Oversee spend for 15+ clinical and 20+ lab programs, tracking forecasts, budgets, and actuals across outsourced contract manufacturing streams.
- Business Partnering: Proactively engage with US and global program leads to capture shifts in business drivers, costs, and timelines, using these insights to enrich Quarter Close commentary.
- Financial Planning & Reporting: Handle clinical/development spend movement analysis, payroll and related cost tracking (staff and contingent workers), and 6-monthly Sweep Allocations to Net Expense and COGM.
- Month/Quarter Close: Ownership of key month-end processes including prepayments, accruals, sweep certifications, and P&L Net Expense variance analysis.
- Systems & Transformation: Utilize Smartsheet for project tracking and SAP GL for accounting, while supporting upcoming system transitions (Anaplan and S4/HANA).
- Compliance & Governance: Ensure all accounting entries meet US GAAP and SOX requirements, managing transitions from pre-commercial to commercial stages (90:90 approvals)
- Non-Negotiables & Key RequirementsQualifications: Bachelor's degree or Professional Accounting qualification with 6-8 years of experience in Finance, FP&A, or Operations Finance.
- Core Technical Skills: Proven experience in SAP GL and program spend/budget management across dynamic environments.
- Industry Focus: Post-qualification experience in a multi-national environment. Prior Biotech, Pharmaceutical, or regulated manufacturing experience is strongly preferred due to specific terminology (e.g., PPQ, CTM).
- System Knowledge: Proficiency with Smartsheet, Ariba, Hyperion, and Microsoft Office (Excel, PowerPoint).
- Schedule Flexibility: Willingness to work outside core hours to support program owners in US time zones.
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