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ICON plc
ICON plc
Asistență medicalăConsultanțăLogistică
ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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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.

TRTurciaRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • 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

Cerințe

  • 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

Beneficii

  • 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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