Global Study Management (Senior) Associate (Global CTA)

📋 Description

• Support global clinical study delivery with quality, timelines and budgets in an oncology setting.
• Coordinate cross-functional Clinical Study Team meetings with global/regional stakeholders.
• Support study setup and maintenance across systems (eTMF, CTMS) and study-level info.
• Develop and maintain study plans, tools, and study documentation.
• Review clinical study documents (protocols, ICFs, IBs, monitoring plans, CRFs).
• Organize investigator meetings and support site feasibility activities.

🎯 Requirements

• Bachelor’s degree or higher in a scientific/healthcare field; advanced degree preferred.
• At least 3 years of clinical research experience in biotech/pharma/CRO.
• Solid understanding of clinical operations and regulatory requirements (ICH-GCP).
• Strong proficiency with Microsoft Office (Excel, PowerPoint, Project).
• Excellent organizational and coordination skills; detail-oriented and collaborative.
• Ability to manage multiple activities, priorities and deadlines; good communication across

🎁 Benefits

• Market-competitive compensation package.
• Performance-based annual bonus opportunity.
• Company shares including a welcoming grant.
• Learning and development opportunities; comprehensive benefits program.
• Opportunity to work with an international, collaborative team.
• Exposure to global clinical development and oncology research.