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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 - France Remote | ICON plc

Senior Clinical Research Associate overseeing clinical trial monitoring for ICON plc’s sponsor-dedicated research programs in France. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.

FRFranțaRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead technically complex monitoring work while advancing quality and process improvement
  • Evaluate clinical trial sites against protocols, regulations, and Good Clinical Practice requirements
  • Conduct site visits, address operational issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site staff and fellow Clinical Research Associates
  • Develop strong working relationships with site teams and stakeholders to support efficient trial operations

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial Clinical Research Associate experience with strong knowledge of trial operations and regulatory requirements
  • Demonstrated ability to coordinate multiple sites and projects, supported by strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial systems and tools
  • Strong communication, interpersonal, and stakeholder-management abilities, with the influence needed to promote compliance in a complex setting
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the position is located

Beneficii

  • Competitive base pay with performance-based incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension arrangements
  • Life assurance and disability protection
  • Employee assistance programmes and wellbeing support
  • Professional development through structured training and career progression pathways

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