ICON plc
ICON plc
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.

Senior Clinical Research Associate - Turkey (Remote)

Senior Clinical Research Associate role at ICON plc supporting sponsor-dedicated clinical trials in Turkey. The position focuses on protocol compliance, site performance, data quality, and regulatory standards.

Description

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with an emphasis on quality and continuous improvement
  • Assess clinical sites for compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, address issues, and support successful trial delivery
  • Work with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and guide site staff and fellow Clinical Research Associates
  • Develop stakeholder relationships that support efficient trial operations

Requirements

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with strong knowledge of trial processes and regulatory requirements
  • Demonstrated ability to oversee multiple sites and projects while applying strong organizational and problem-solving skills
  • Advanced knowledge of monitoring, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder-management skills, with the ability to influence compliance in complex environments
  • Availability to travel as needed, approximately 60%
  • Legal authorization to work in the country where the position is based

Benefits

  • Competitive base pay with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career development opportunities

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