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Lead complex, cross-functional HR programs from initiation through implementation. Establish governance, manage dependencies, risks, and multiple concurrent initiatives. Drive stakeholder alignment and influence senior leaders, produce executive communications, and standardize HR project methodologies, tools, and governance. Serve as a trusted advisor on high-visibility, ambiguous initiatives.

Prepare, analyze, and deliver financial reports, budgets, forecasts, and metrics for assigned areas. Investigate financial results, produce monthly commentary, support cost and revenue analyses, build subject visit forecasts using protocol/subject data, and provide insights on profitability and growth. Support ad-hoc reporting and finance projects.

Support Business Unit Controller by recording monthly revenue, loading and maintaining project budgets in Oracle/Revenue Wizard, preparing monthly actual vs. budget variance and backlog forecasts, drafting financial reports, performing project close-out reconciliations, and monitoring project health (revenues, gross profit, receivables, unbilled). Attend project meetings to capture setup data and ensure forecast accuracy.

Prepare and compile invoice packages from monthly data, create invoices in Oracle, save and distribute invoice PDFs or hard copies, update the billing repository, respond to invoice queries, process credits/rebills, and provide details for journal corrections.

Analyze HR metrics (headcount, attrition, hiring), create executive-ready PowerPoint decks, convert data into visual stories and recommendations, build and maintain reporting templates, partner with HR/TA/Finance, ensure data accuracy, and support ad hoc analysis and reporting needs.

As a Site Contracts Specialist, you'll manage contracts for clinical trials, including negotiations, quality control, and compliance with regulatory standards while collaborating with internal and external teams.

The Clin Ops Specialist ensures compliance in clinical trials, manages communications with participants, and supports study processes with administrative tasks.

Perform site qualification, monitoring, management, and close-out visits while ensuring regulatory compliance and data integrity. Support subject recruitment and project objectives.

The Sr CRA manages clinical trial processes, ensuring compliance with protocols, training junior staff, and collaborating with teams for data integrity.

The Clinical Trial Supplies Manager oversees the supply chain logistics for clinical trials, ensuring timely delivery and compliance with regulatory standards while collaborating with cross-functional teams.