Site Activation Coordinator

Responsibilities

• Perform site activation activities for assigned studies in accordance with local and international regulations, SOPs, and work instructions.
• Prepare and review site regulatory documents for completeness, consistency, and accuracy.
• Inform team members and project management of the completion of regulatory and contractual documents for individual sites.
• Distribute completed documentation to investigative sites and internal project team members.
• Support the maintenance of internal systems, databases, tracking tools, and project timelines with accurate information.
• Track and follow up on the progress and execution of regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.

Requirements

• Bachelor's Degree in Life Sciences or a related field.
• 1 year of experience in a healthcare environment or clinical research (internship experience is acceptable).
• Proficiency in MS Office applications and word processing.
• General awareness of the clinical trial environment and the drug development process.
• Strong attention to detail and organizational skills.
• Ability to manage multiple projects simultaneously and maintain effective working relationships.
• Ability to work in a hybrid office model.

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.