Associate Clinical Project Manager, Sponsor Dedicated

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout, ensuring high-quality data delivery and regulatory compliance. The role requires expertise in clinical trial management, drafting and managing informed consent processes, and driving risk-based mitigation plans.

Requirements

• Bachelor's Degree In life sciences or related field
• 2 years clinical trial management experience
• Intermediate level knowledge of principles, theories, and concepts of clinical trial management
• Knowledge of clinical trials, clinical trial conduct, and relevant local laws, regulations and guidelines
• Strong written and verbal communication skills
• Problem solving skills
• Planning, time management and prioritization skills
• Ability to handle conflicting priorities
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

Benefits

• Health and welfare benefits
• Incentive plans, bonuses, and/or other forms of compensation