VP Clinical Development
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Resilience is a global, clinical-stage medtech company specializing in oncology, gastroenterology, and psychiatry. We develop digital solutions that transform patient care and generate robust clinical data to improve treatments. As a true sponsor, we are conducting multiple prospective randomized clinical trials to obtain regulatory approvals in Europe and the United States.
Your Role
In a nutshell:
The Vice President, Clinical Development will own and lead all sponsor-led clinical development activities at Resilience across oncology, gastroenterology, and psychiatry.
This role is accountable for the strategic direction, design, and execution of Resilience-sponsored clinical trials and real-world evidence programs, ensuring consistency, scientific rigor, operational excellence, and regulatory readiness across all business units.
Reporting to the Chief Medical Officer, the VP Clinical Development will build and lead a centralized Clinical Development organization, composed of Clinical Leads and Clinical Scientists, and will serve as the single point of accountability for clinical development execution at the company level.
Key Responsibilities
Clinical Development Ownership (Core accountability)
Own the end-to-end clinical development strategy and execution for all Resilience-sponsored studies
Provide senior clinical leadership on:
study design and methodology
protocol development and amendments
endpoint selection and clinical relevance
interpretation of clinical and real-world evidence
Ensure alignment and consistency of clinical development approaches across oncology, gastroenterology, and psychiatry
Team Leadership & Organization
Build, lead, and mentor a Clinical Development team composed of:
Clinical Leads (by therapeutic area)
Clinical Scientists
Define clear roles, responsibilities, and governance across the team
Establish scalable ways of working enabling high-quality, timely execution
Portfolio Governance & Standardization
Design and implement standardized clinical development frameworks across business units
Harmonize:
protocol templates and study documentation
clinical review and governance processes
decision criteria and escalation pathways
Ensure alignment with ICH-GCP, ISO 14155, MDR, and applicable regulatory standards
Operational Excellence & Inspection Readiness
Ensure inspection readiness across all sponsor-led trials
Partner closely with Clinical Operations to:
drive execution excellence and risk anticipation
ensure quality-by-design principles
resolve complex operational or scientific issues
Act as senior escalation point for clinical development matters
Cross-Functional Leadership
Collaborate closely with:
Regulatory & Quality (clinical strategy, submissions, audits)
Biostatistics (study design, endpoints, analysis plans)
Medical Affairs (scientific alignment and evidence narratives)
Market Access & Public Affairs (clinical evidence support)
Product and Data teams (translation of clinical insights into digital solutions)
Ensure clinical development is tightly integrated with company-wide priorities
Candidate Profile
You're the right person if you are:
A strategic thinker with the ability to prioritize in complex environments
An inspiring leader with a talent for developing your teams
Executive presence with strong scientific credibility<
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