Study Management Senior Manager, Obesity – US, Remote

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Requirements:

• Basic Qualifications: Doctorate degree and 2 years of Clinical Research experience OR Master's degree and 4 years OR Bachelor's degree and 6 years OR Associate's degree and 10 years OR High school diploma / GED and 12 years of Clinical Research experience.
• Preferred Qualifications: 9 years of work experience in life sciences or a related field, including 6 years of biopharmaceutical clinical research experience.
• Experience managing outside clinical research vendors and leadership experience managing direct reports.

Responsibilities:

• Support continuous improvement initiatives in Clinical Program Operations and Global Development Operations.
• Coordinate and oversee operational strategy, planning, risk assessment, and overall delivery of clinical trial programs globally.
• Line management of GTMs and support for the CPO Director/Sr. Director, leading smaller programs in their absence.
• Ensure high-quality delivery of clinical trials on time and within budget.
• Lead the Global Clinical Study Team for allocated programs.
• Provide clinical operations leadership on the Evidence Generation Team and in the development of the Evidence Generation Plan.
• Oversee clinical program budgets in collaboration with Therapeutic Area and Finance.
• Manage program-level operational issues and issue escalation.
• Maintain cross-functional global business relationships and communicate trial program status to senior management.
• Represent the CPO on process improvement initiatives.
• Support CPO resource planning in collaboration with Program Resource Management and CPM-D.