Support clinical study operations as a Project Coordinator II by coordinating site activation and facilitating effective communication among teams. Ensure timely and accurate documentation for projects.
This position calls for 1 to 2 years of relevant experience in clinical research, equipped with strong organizational skills and a comprehensive understanding of GCP and ICH guidelines. You will take ownership of deliverables, coordinate site activities, and support regulatory submissions. Your communication skills will be vital in managing interactions with internal and external stakeholders.
Key Responsibilities:
• Coordinate essential documentation for site activation
• Prepare reports and meeting minutes for stakeholders
• Assist with ethics committee submissions when necessary
• Manage logistics for investigator meetings and supplies
• Support audits and provide necessary documentation
Requirements:
• Bachelor’s degree in clinical research or related fiel...