Turkey, Istanbul, Türkiye Hybrid Full-time

ICON plc is hiring a Clinical Research Associate 3

About the Role

What You'll Do

Oversee clinical trial sites to verify adherence to study protocols, regulatory guidelines, and Good Clinical Practice. Conduct regular on-site and remote visits to evaluate performance, identify gaps, and implement corrective actions. Support trial execution by working closely with study teams to ensure data is collected accurately and reported on schedule. Provide guidance to site staff and fellow monitors to uphold rigorous standards in trial conduct. Foster strong working relationships with site personnel and key stakeholders to promote efficient operations and sustained engagement throughout the study lifecycle.

Requirements

Hold an advanced degree in a life science, nursing, or medical field. Bring substantial experience as a Clinical Research Associate with a solid grasp of clinical trial design, execution, and regulatory expectations. Demonstrate consistent success managing multiple sites and studies under tight timelines, using strong organizational and critical-thinking abilities. Show proficiency in clinical monitoring, data quality assurance, and site management, along with experience using clinical trial management systems and related software tools. Communicate clearly and effectively with cross-functional teams and external partners. Possess a valid driver’s license and be prepared to travel frequently—approximately 60% of time, including domestic and international trips involving both flying and driving.

Benefits

Receive a competitive salary and comprehensive benefits package tailored to support your long-term well-being. Choose from a variety of health insurance plans designed to meet diverse needs for you and your family. Benefit from generous retirement planning options that help secure your future. Access 24/7 support through a global employee assistance program offering confidential counseling and wellness resources. Life assurance is included as part of core benefits. Additional country-specific options may include childcare subsidies, bike purchase programs, discounted gym access, subsidized transit passes, and preventive health screenings.

Work Mode

This role operates in a hybrid model with significant travel required—approximately 60% of time spent on the road, including both domestic and international destinations. Flexibility to travel and conduct site visits by air and car is essential to success in this position.

Required Skills
clinical trial softwaredata integritysite managementregulatory compliancemonitoring practicesproject managementstakeholder managementproblem-solvingorganizational skillscommunication skills clinical trial softwaredata integritysite managementregulatory compliancemonitoring practicesproject managementstakeholder managementproblem-solvingorganizational skillscommunication skills
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About company
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization.
All jobs at ICON plc Visit website
Job Details
Category other
Posted 8 days ago