Compliance and Risk Management Lead
• *Overview**
We are seeking an experienced professional to support compliance, regulatory oversight, and risk management activities across clinical trials. This is a newly created position focused on ensuring adherence to regulatory standards and proactive risk identification and mitigation.
Key Responsibilities
• Oversee clinical trial compliance with applicable regulatory requirements and internal standards
• Lead risk management and risk assessment processes across studies
• Identify, evaluate, and mitigate operational and regulatory risks
• Partner with internal stakeholders to ensure alignment with compliance frameworks
• Support governance processes and ensure proper documentation and audit readiness
• Provide guidance on clinical trial best practices and regulatory expectations
Qualifications
• 8–10 years of experience
in clinical trials, ideally in compliance, regulatory, or risk management roles
• Strong understanding of global regulatory requirements and clinical trial processes
• Experience within
• *pharma or a mix of pharma/CRO environments strongly preferred**
• CRO-only backgrounds will be considered if initial candidate pool is limited
• Proven ability to work cross-functionally and influence stakeholders
• Strong analytical and problem-solving skills
We are seeking an experienced professional to support compliance, regulatory oversight, and risk management activities across clinical trials. This is a newly created position focused on ensuring adherence to regulatory standards and proactive risk identification and mitigation.
Key Responsibilities
• Oversee clinical trial compliance with applicable regulatory requirements and internal standards
• Lead risk management and risk assessment processes across studies
• Identify, evaluate, and mitigate operational and regulatory risks
• Partner with internal stakeholders to ensure alignment with compliance frameworks
• Support governance processes and ensure proper documentation and audit readiness
• Provide guidance on clinical trial best practices and regulatory expectations
Qualifications
• 8–10 years of experience
in clinical trials, ideally in compliance, regulatory, or risk management roles
• Strong understanding of global regulatory requirements and clinical trial processes
• Experience within
• *pharma or a mix of pharma/CRO environments strongly preferred**
• CRO-only backgrounds will be considered if initial candidate pool is limited
• Proven ability to work cross-functionally and influence stakeholders
• Strong analytical and problem-solving skills