Risk Manager (Clinical Research)

📋 Description

• Provide subject matter expertise in developing, implementing, and updating risk-based monitoring
• Collaborate with cross-functional teams to identify, assess, characterize, and mitigate risks
• Coordinate with central monitoring teams when required and review their work to ensure quality and
• Provide budget recommendations and support the preparation of change orders when project
• Draft initial risk assessments and contribute to the completion of Risk Assessment and
• Guide project managers in transferring identified risks into appropriate tracking systems and

🎯 Requirements

• Bachelor’s degree in a discipline relevant to clinical research.
• Mandatory professional experience within a Contract Research Organization (CRO) or pharmaceutical
• At least 3 years of experience in risk management within a clinical research environment.
• At least 5 years of experience across clinical monitoring, data management, and/or drug safety.
• Strong knowledge of Good Clinical Practice (GCP), ICH E6 (R3) guidelines, and applicable regulatory
• Demonstrated expertise in Risk-Based Monitoring (RBM) strategies, processes, and tools.

🎁 Benefits

• Permanent, full-time employment.
• Flexible work schedule.
• Ongoing learning and professional development opportunities.
• Stimulating and collaborative work environment.
• Opportunities for career growth and advancement.