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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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Clinical Site Manager II – Beijing (Hybrid)

Lead site monitoring, compliance, and trial delivery for ICON plc’s sponsor-dedicated clinical research programs in China.

CNChinaHibridNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăOperațiuni clinice
Google Cloud Platform

Descriere

  • Direct clinical trial operations in line with study protocols, regulations, and industry standards
  • Take ownership of technically complex monitoring activities while advancing quality and continuous improvement
  • Verify that study sites follow protocols, regulatory obligations, and Good Clinical Practice (GCP) requirements
  • Visit sites to evaluate performance, address issues, and help keep trials on track
  • Partner with cross-functional teams to support accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with investigators, site teams, and other stakeholders
  • Coordinate multiple sites and projects concurrently

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Substantial Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory requirements
  • Demonstrated success managing several sites and projects at once, supported by strong organization and problem-solving abilities
  • Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder-management capabilities, with the ability to influence 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 programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension benefits
  • Life assurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Professional development through structured training and career progression pathways

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