Vice President, Clinical Operations
Company: iBio, Inc.
Role summary
Vice President, Clinical Operations is a full-time role at iBio, Inc. in San Diego, California, United States (on-site). Posted 2026-10-10. Salary: USD 267,417–354,483 per year. Experience level: 10+.
- Job title
- Vice President, Clinical Operations
- Company
- iBio, Inc.
- Location
- San Diego, California, United States
- Work arrangement
- on-site
- Employment type
- full-time
- Category
- Healthcare Support
- Salary
- USD 267,417–354,483 per year
- Experience level
- 10+
- Date posted
- 2026-10-10
This is a fantastic opportunity to lead clinical operations at an innovative, AI-driven biotech company focused on groundbreaking therapies. You'll play a crucial role in accelerating drug development, with a highly competitive salary and the chance to make a real impact.
Job description
Description
About iBio
iBio is an AI-driven innovator developing therapies for cardiometabolic, obesity and cardiopulmonary diseases. iBio’s mission is to decrease drug failures, shorten development timelines, and open up new frontiers against the most promising therapeutic targets. iBio is based in San Diego, CA. For more information, visit www.ibioinc.com .
The Opportunity
Join iBio as Vice President, Clinical Operations!
iBio is seeking an accomplished and forward-thinking Vice President, Clinical Operations to join our leadership team and play a pivotal role in advancing our clinical development pipeline.
This is an exciting opportunity for a strategic leader to shape and scale our Clinical Operations function, build a high-performing team, and drive operational excellence across our clinical programs. Working closely with the Chief Medical Officer and cross-functional leaders, the successful candidate will help translate our clinical development strategy into effective execution and build the capabilities needed to support iBio’s continued growth.
If you are passionate about building high-performing teams, driving clinical execution, and making a meaningful impact in biotechnology, we invite you to explore this opportunity.
Location: Onsite — Sorrento Valley, San Diego, CA
Responsibilities:
Clinical Operations Leadership & Strategy
Provide strategic leadership and overall accountability for Clinical Operations, aligning priorities, capabilities, resources, and operating models with the company’s clinical development strategy and growth.
Serve as a senior member of the leadership team, providing Clinical Operations expertise and strategic input on portfolio, program, organizational, and operational decisions.
Clinical Development & Trial Operations
Provide strategic oversight of clinical development programs and trials, ensuring high-quality, timely, compliant, and efficient execution.
Partner with cross-functional teams to identify and manage operational risks, establish priorities, and support successful delivery of clinical programs.
Organization & Team Development
Build and lead a high-performing Clinical Operations organization, establishing the structure, capabilities, and talent needed to support the company’s evolving clinical pipeline.
Recruit, develop, and retain talent while fostering a culture of accountability, collaboration, quality, innovation, and continuous improvement.
Quality & Operational Excellence
Establish and oversee an effective Clinical Operations quality framework, including the Quality Management System (QMS), SOPs, processes, training, governance, and inspection readiness.
Drive continuous improvement in Clinical Operations processes, systems, and ways of working to enhance quality, efficiency, scalability, and risk management.
External Partnerships & Cross-Functional Leadership
Develop and oversee strategic relationships with CROs, clinical vendors, investigators, sites, consultants, and other external partners to support effective program execution.
Partner closely with the CMO and cross-functional leaders to advance clinical programs, align priorities, and make informed decisions regarding timelines, resources, risks, and operational strategy.
Resources, Budget & Governance
Provide strategic oversight of Clinical Operations budgets, resources, systems, and infrastructure, balancing quality, timelines, cost, capacity, and operational risk.
Establish appropriate governance, performance metrics, and reporting mechanisms to support visibility, accountability, informed decision-making, and effective execution across Clinical Operations.
Additional Responsibilities
Provide Clinical Operations leadership and expertise in clinical development planning, strategic initiatives, and organizational priorities, serving as a strategic advisor to executive leadership.
Establish and monitor key performance indicators, operational metrics, and risks to support informed decision-making and continuous improvement.
Partner with cross-functional leaders and represent Clinical Operations with external stakeholders, including CROs, vendors, investigators, consultants, and other strategic partners.
Maintain awareness of evolving clinical development practices, regulatory expectations, technologies, and industry trends, identifying opportunities to strengthen the company’s clinical development capabilities.
Perform other duties consistent with the scope and level of the role.
Supervisory Responsibilities
Lead and develop the Clinical Operations organization, establishing clear priorities, roles, objectives, and accountability aligned with the company’s clinical development strategy.
Recruit, coach, develop, and retain high-performing talent while building organizational capabilities and future leadership to support the company’s growth.
Foster a culture of accountability, collaboration, quality, compliance, scientific and operational rigor, innovation, and continuous improvement.
Requirements
Education & Experience
Bachelor’s degree with 15+ years of progressive experience, or Master’s degree with 13+ years of progressive experience, in Clinical Operations, Clinical Development, clinical research, or a related field within biotechnology, pharmaceutical, or life sciences.
Hands-on Phase 1 and Phase 2 clinical trial experience within a small or emerging biotechnology company, preferably using an outsourced/CRO operating model.
Progressive leadership experience, including experience building, leading, and developing high-performing Clinical Operations teams.
Demonstrated experience leading clinical trials and clinical development programs, with a strong understanding of ICH/GCP and applicable regulatory requirements.
Experience building and scaling Clinical Operations infrastructure, including processes, SOPs, quality systems, vendors, and operational capabilities.
Experience selecting and managing CROs and clinical ve