Remote VP, Clinical & Industry Trials - Strategy & Ops

CommonSpirit Health; United States; Remote; USD 240,000 - 360,000; Full time

Benefits offered by this job

Work from home equipment provided

Remote work flexibility

Job summary

CommonSpirit Health seeks a System Vice President, Clinical and Industry Trials to lead the health system's clinical trial enterprise and align it with the system's research strategy. You will oversee investigator-initiated and industry-sponsored trials, manage regulatory compliance, budgeting, contracting, and performance metrics across sites.

You will collaborate with external sponsors and internal partners, ensuring efficient trial activation, patient recruitment, and data integrity while

Qualifications

• Proven track record leading clinical research programs and trial operations.
• Experience overseeing budgeting, contracting, and performance metrics for trials.
• Ability to collaborate with sponsors, regulatory bodies, IRBs, and institutional leadership.

Responsibilities

• Develop a short-term strategy for clinical and industry trials aligned with the system research mission.
• Oversee regulatory compliance, budgeting, contracting, and performance metrics across trials.
• Ensure efficient trial activation, patient recruitment, and data integrity across sites.
• Lead efforts to streamline processes and adopt digital tools for trial management.
• Promote efficiency and quality through innovation and change management in trials.
• Collaborate with legal/compliance and executive leaders to align strategies with the mission.

Skills

Strategic leadership

Clinical trial operations

Regulatory compliance

Stakeholder engagement

Job description

CommonSpirit Health seeks a System Vice President, Clinical and Industry Trials to lead the health system's clinical trial enterprise and align it with the system's research strategy. You will oversee investigator-initiated and industry-sponsored trials, manage regulatory compliance, budgeting, contracting, and performance metrics across sites.

You will collaborate with external sponsors and internal partners, ensuring efficient trial activation, patient recruitment, and data integrity while