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We are looking for a Site Activation Coordinator to join our team in Romania and provide support in the country about the activities related with activation of site (preparation of documents, follow ups and be involve in new projects).

Your responsabilities

• Prepare site regulatory documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory and contractual documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Your Profile

• Bachelor Degree in Lifescience or related field.
• Valuable experience in clinical trials or medical field.
• Romanian and English Proficient level.
• Microsoft Office user (Excel, Outlook).
• Availability to go to the office (Bucharest).
• Communication and organizational skills.

We are offering the possibility to join the team move your career into further steps. Permanent contract and benefits of being an IQVIAN.

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. Learn more at https://jobs.iqvia.com