ICON plc
ICON plc
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.

Clinical Site Manager II – China (Remote)

Lead clinical trial site management for ICON plc in China, supporting protocol compliance, data integrity, and effective study execution. The role covers site oversight and collaboration across Beijing and Shanghai.

Descriere

  • Lead technically complex clinical trial monitoring activities with an emphasis on quality improvement
  • Evaluate sites against study protocols, regulatory obligations, and Good Clinical Practice standards
  • Perform site visits to review performance, address issues, and support successful study delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and coach site personnel and fellow Clinical Research Associates
  • Develop productive working relationships with site teams and other key stakeholders

Cerințe

  • Hold a bachelor's degree in a relevant scientific or healthcare discipline
  • Bring extensive Clinical Research Associate experience and a strong grasp of clinical trial operations and regulatory requirements
  • Demonstrate the ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Have advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with relevant clinical trial software and tools
  • Communicate effectively with stakeholders and use strong interpersonal and relationship-management skills to promote compliance in complex settings
  • Be prepared to travel as needed, approximately 60% of the time
  • Have the legal right to work in the country where the position is based

Beneficii

  • Base salary with performance-linked incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension provisions
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Professional development through structured training and career progression pathways

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