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Join Our Team at IQVIA Zagreb!

Are you passionate about making a difference in the clinical research field? IQVIA Zagreb is excited to welcome a dedicated and dynamic (Sr) Site Activation Specialist to our team of professionals.

Job Overview:

• Ensure all site documents are complete and accurate.
• Distribute documents to sites and internal project teams.
• Review, track, and follow up on the progress, approval, and execution of essential documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Forms (ICFs), and Investigator Pack (IP) release documents.
• Manage EDP collection and site readiness for enrollment activities.
• Negotiate investigator budgets and site Clinical Trial Agreements.

Qualifications:

• Bachelor's degree in Life Sciences (preferred).
• Over 2 years of relevant clinical site activation experience, including managing clinical trial contracts and submissions to EC/RA in Croatia and Slovenia (experience in Bosnia is a plus).
• Desirable but not crucial: Site ID experience.
• Proficiency in Croatian and English.
• Based in Croatia, with the flexibility to work from our Zagreb office or in a hybrid mode.
• A passion for growing your career long-term within our Clinical Site Activation department.

If you're ready to take your career to the next level and be part of a team dedicated to advancing healthcare, we want to hear from you!

Apply Now and join us in making a positive impact on global health!

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