Job Description
- *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
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