Applyđź“Ť US
🧠Full-Time
đź’¸ 153550 - 179118 USD per year
🔍 Biotechnology
- 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.
- 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.
LeadershipPeople ManagementCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaboration
Posted 2024-09-22
Apply