Associate, Study Management III/CTM III

Role Overview:

• You will be part of a dynamic, centralized study management team responsible for executing global clinical trials.
• You will work independently to plan, execute, and manage Phase 0-4 clinical trials under guidance.

Key Responsibilities:

• Provide study-level oversight and leadership for global trials from inception to closure.
• Manage vendor selection, scope of work, and risk management.
• Drive recruitment strategies and ensure inspection readiness.

Qualifications & Skills:

• Bachelor’s degree with at least 4 years of progressive clinical research experience.
• Proficient in systems like EDC, IRT, CTMS, and eTMF.
• Strong analytical, organizational, and interpersonal skills.