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The Senior Accountant, General Ledger maintains accurate financial records through journal entries, reconciliations, financial statement disclosures, variance analysis, and clinical trial accounting. The role supports GAAP and IFRS compliance, SOX controls, audits, SOPs, process improvements, and cross-functional collaboration with Clinical Operations and FP&A. It also provides accounting guidance, supports financial reporting, and helps improve scalable finance processes.

Supports the Legal Team with end-to-end commercial contract management, including drafting, redlining, negotiation, execution, renewals, amendments, filing, tracking, and process administration. Maintains contract systems, templates, SOPs, and policies; collaborates with internal and external stakeholders; supports M&A, financing, due diligence, corporate governance, and regulatory compliance activities. The role is onsite in Dunkirk, New York.

Designs and operates secure, scalable infrastructure and deployment platforms. Responsibilities include infrastructure as code, CI/CD pipelines, Kubernetes workloads, container security, observability, vulnerability scanning, access controls, incident management, documentation, and operational support. The role collaborates with development, QA, product, and security teams while maintaining compliance, change control, SOPs, and reliable production services.

Responsible for general ledger accounting, journal entries, reconciliations, financial statements, fixed assets, variance analysis, GAAP compliance, SOX controls, audits, and accounting process improvements. Supports ERP implementations, internal controls, policy consistency, and scalable financial processes while managing competing priorities and cross-functional projects.

The Regulatory Affairs Program Manager leads cross-functional regulatory projects, ensuring products meet global regulatory requirements and are launched on schedule.

Configure, maintain, and optimize the company's Workday system (HCM, Compensation, Talent, Learning, Absence). Provide day-to-day support, troubleshoot data/system issues, build custom reports and dashboards, ensure data integrity, support updates/releases, and partner with HR on process improvements and change management.

Manage daily contract lifecycle activities including intake, drafting and finalizing routine agreements, routing for electronic signatures, maintaining CLM repository metadata and version control, tracking milestones and renewals, generating pipeline reports, supporting corporate filings and entity records, and collaborating with procurement and legal teams to ensure compliance and timely execution.

The Senior Specialist in Regulatory Affairs will develop compliance strategies, prepare documents, maintain regulations, and keep updated with regulatory trends.

The Veeva RIM Specialist manages and publishes regulatory documents using Veeva RIM software, ensuring compliance with health authority requirements and supporting submission activities for regulatory affairs.

The Senior Clinical Data Manager oversees clinical trial databases, mentors junior staff, and ensures data quality and compliance with regulatory standards.