Join IQVIA as a Senior Clinical Research Activation Specialist, where you will handle essential site activation tasks in a cooperative setting. Utilize your expertise to enhance clinical trial processes and outcomes.
In this role, you function under general supervision, facilitating critical site activation activities while ensuring compliance with regulations and SOPs. As the Single Point of Contact, you streamline communications between investigative sites and internal project teams. You’ll conduct feasibility studies, review site documentation, and provide feedback based on performance metrics.
Key Responsibilities:
• Ensure compliance with regulations and project timelines
• Review and prepare site documents for accuracy




• Track progress of essential project documents
• Provide feedback on site performance metrics
• Collaborate with teams for effective project execution
Requirements:
• Bachelor’s Degree in Life Science or similar
• Minimum 3 years of clinical research experience
• 1 year leadership experience in clinical settings
• Familiarity with standard operating procedures
• Excellent organizational and communication skills
Your contributions will help shape the future of clinical research at IQVIA.
J-18808-Ljbffr

📌 Senior Clinical Research Activation Specialist Toronto (Canada)
🏢 IQVIA
📍 Canada