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 quick-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.

📌 CTA Professional (New Delhi)
🏢 Naukri Healthcare Jobs
📍 New Delhi