Unlock potential by leading global clinical trials across EMEA and LATAM. Ensure exceptional study execution through cross-functional collaboration, regulatory compliance, and operational excellence in oncology and neuroscience sectors.

Engage in the strategic management of enterprise IT systems, optimizing infrastructure and enhancing operational efficiency while leading cross-functional teams and mentoring junior staff in a fast-paced biotechnology environment.

Drive clinical quality assurance by leading GCP audits, ensuring compliance, mentoring teams, and developing risk-based audit plans to uphold the highest quality standards in clinical trials and stakeholder collaboration.

Lead, develop, and execute comprehensive GCP auditing programs, ensuring clinical trials meet regulatory standards, while guiding and mentoring teams in a collaborative, dynamic environment for exceptional quality assurance results.

Develop and drive regulatory strategy for clinical-stage programs, ensuring compliance with FDA and international guidelines. Collaborate with cross-functional teams to navigate complex regulatory landscapes and support product development efficiently.