Job Description

Locations

• Turkey, Istanbul

Skills Required

• GCPintermediate
• Microsoft Wordintermediate

Required Qualifications

• Bachelor’s degree in a scientific or healthcare discipline, or equivalent experience. (experience)
• Minimum of 1 year of on-site monitoring experience. (experience, 1 years)
• Good knowledge of GCP, ICH guidelines, and clinical research processes. (experience)
• Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools. (experience)
• Strong written and verbal communication skills in English. (experience)
• Excellent organizational, time‑management, and problem‑solving abilities. (experience)
• Ability to build strong working relationships with sites, colleagues, and sponsors. (experience)
• Bachelor’s degree in a scientific or healthcare discipline, or equivalent experience. (experience)
• Minimum of 1 year of on-site monitoring experience. (experience, 1 years)
• Good knowledge of GCP, ICH guidelines, and clinical research processes. (experience)
• Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools. (experience)
• Strong written and verbal communication skills in English. (experience)
• Excellent organizational, time‑management, and problem‑solving abilities. (experience)
• Ability to build strong working relationships with sites, colleagues, and sponsors. (experience)
• 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 (experience)
• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. (experience)

Responsibilities

• Conduct selection, initiation, monitoring, and close‑out visits according to GCP, ICH guidelines, and the contracted scope of work.
• Work with sites to develop and track subject recruitment plans aligned with project timelines.
• Provide protocol and study‑specific training to site personnel; maintain regular communication to support expectations and resolve issues.
• Assess site performance and ensure adherence to protocol, study procedures, and regulatory compliance; escalate quality issues when appropriate.
• Track study progress (regulatory submissions, approvals, enrollment, CRF completion, and data queries) and support start‑up activities when needed.
• Ensure essential documents are properly maintained in the TMF and verify ISF compliance with GCP and local regulatory standards.
• Document site management activities through timely monitoring visit reports, follow‑up letters, and required study documentation.
• Collaborate with cross‑functional study team members to support operational excellence.
• When applicable, support site-level recruitment planning and site financial management.
• Conduct selection, initiation, monitoring, and close‑out visits according to GCP, ICH guidelines, and the contracted scope of work.
• Work with sites to develop and track subject recruitment plans aligned with project timelines.
• Provide protocol and study‑specific training to site personnel; maintain regular communication to support expectations and resolve issues.
• Assess site performance and ensure adherence to protocol, study procedures, and regulatory compliance; escalate quality issues when appropriate.
• Track study progress (regulatory submissions, approvals, enrollment, CRF completion, and data queries) and support start‑up activities when needed.
• Ensure essential documents are properly maintained in the TMF and verify ISF compliance with GCP and local regulatory standards.
• Document site management activities through timely monitoring visit reports, follow‑up letters, and required study documentation.
• Collaborate with cross‑functional study team members to support operational excellence.
• When applicable, support site-level recruitment planning and site financial management.

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