CTA Professional

Roles and Responsibility

• Manage and coordinate clinical trial activities, including protocol development, site monitoring, and data analysis.
• Develop and implement regulatory strategies to ensure compliance with relevant laws and regulations.
• Collaborate with cross-functional teams, including medical writing, quality assurance, and IT to achieve project goals.
• Conduct risk assessments and develop mitigation plans to minimize risks associated with clinical trials.
• Ensure timely and within-budget delivery of projects, while maintaining high-quality standards.
• Provide training and guidance to junior staff members on clinical trial conduct and regulatory affairs.

Job Requirements

• Strong knowledge of clinical trials, regulatory affairs, and quality assurance principles.
• Excellent communication, project management, and interpersonal skills.
• Ability to work effectively in a fast-paced environment with multiple priorities and deadlines.
• Strong analytical and problem-solving skills, with attention to detail and accuracy.
• Experience with medical writing, CTMS (Clinical Trials Management System), and other relevant software applications.
• Bachelor's degree in a related field such as biology, pharmacy, or medicine.