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IQVIA Zagreb is looking for a new team member to join our team of professionals as a (Sr) Site Activation Specialist.

Job Overview:

• Perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy.
•  Prepare site documents, reviewing for completeness and accuracy.
• Distribute completed documents to sites and internal project team members.
• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.
• Clinical Trial Agreement (CTA) negotiations.

Qualifications:

• Bachelor's Degree in Life sciences preferred.
• 2+ years’ of relevant clinical site activation experience, including clinical trial contracts management.
• Available to work from office in Zagreb, Croatia or in a hybrid mode, Croatia located.
• Fluent in both Croatian and English language.

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