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IQVIA, located in Fatih, Turkey, is seeking a Site Activation Coordinator to perform crucial tasks at a country level related to site activation activities. This role involves ensuring compliance with regulations and maintaining documents for clinical trials to provide patients with access to safe medication.
The ideal candidate will have a Bachelor's Degree in Life Sciences, at least two years of experience, and excellent interpersonal skills to work efficiently with various teams. This position offers exposure across numerous projects and a vibrant working environment.
Make an impact on patient health!
IQVIA’s Global Site Activation Team of 2000 employees drives best‑in‑class site and customer experience, with industry-leading outcomes.
We keep the patient at the forefront; “Always Impatient for the Patient” and we excel in our collaboration with external/internal customers.
IQVIA’s Country Site Activation team is a global network that identifies and activates sites to the highest quality to ensure patients on clinical trials have access to safe and effective medication.
We are leaders in innovation and first to new technologies, providing career development opportunities.
As a Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities.
These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
You will 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, Project Management team, and other departments as necessary.
Coupled with reviewing documents for completeness, consistency, and accuracy, under guidance of senior staff, you will prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and investigator pack release documents.
You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project‑specific information.
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting‑edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.