Global Site Budgets & Payments Ops Leader

MSD; Rahway (NJ); On-site; USD 173,000 - 273,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision care

Retirement benefits (e.g., 401(k))

Paid holidays and vacation

Job summary

MSD is seeking a Head of Site Budgets & Payments Operational Excellence to lead end-to-end budget and payment processes across global sites, ensuring architecture, governance, analytics and enablement align with regional needs. You will partner with Finance, Tax, Compliance and regional teams to standardize capabilities and drive efficiency and compliance.

Ideal candidates bring 10+ years in clinical research operations, strong leadership, and proven ability to translate requirements into

Qualifications

• 10+ years of clinical research experience in the pharmaceutical/biotech industry.
• Experience leading operational teams and driving business outcomes in complex environments.
• Strong collaboration, stakeholder management, and leadership skills.

Responsibilities

• Own the global Site Budgets & Payments Operational Excellence capability and governance across budgets and payments processes.
• Serve as senior authority for end-to-end process stewardship across Site Budgets and Site Payments.
• Establish and maintain globally consistent end-to-end process architecture, governance, and change control.

Skills

Clinical Trial Management

Clinical Trials Operations

Strategic Thinking

Stakeholder Analysis

Relationship Management

Organizational Leadership

Process Improvements

Strategic Analysis

Executive Presence

Business Decisions

ICH GCP Guidelines

Motivating People

Strategic Development

Education

Bachelor's degree

Job description

MSD is seeking a Head of Site Budgets & Payments Operational Excellence to lead end-to-end budget and payment processes across global sites, ensuring architecture, governance, analytics and enablement align with regional needs. You will partner with Finance, Tax, Compliance and regional teams to standardize capabilities and drive efficiency and compliance.

Ideal candidates bring 10+ years in clinical research operations, strong leadership, and proven ability to translate requirements into