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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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Client Services Associate II - Clinical Trials - ICON plc - Shanghai Hybrid

Support patient-centred clinical trial delivery for ICON plc in a hybrid Shanghai role. Coordinate client relationships, project milestones, data analysis, and trial operations.

CNChinaHibridNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăReprezentant Servicii CliențiServicii pentru clienți

Descriere

  • Support patient-centred solutions and take ownership of assigned deliverables in a collaborative team.
  • Work with clients to understand their needs and provide support throughout the clinical trial lifecycle.
  • Coordinate clinical trial activities and track timelines, milestones, and project progress.
  • Connect internal teams and clients to maintain clear communication and effective execution.
  • Analyse data and prepare reports that inform project decisions.
  • Identify operational risks early and help implement solutions to keep projects running smoothly.

Cerințe

  • Bachelor’s degree in life sciences, healthcare, business administration, or a related discipline.
  • At least two years of experience in client services, project management, or clinical research coordination.
  • Strong interpersonal and written and verbal communication skills for working with clients and internal teams.
  • Well-organised and detail-oriented, with the ability to manage multiple priorities concurrently.
  • Proficiency with Microsoft Office applications.
  • Experience with clinical trial management systems is preferred.
  • Availability to travel as needed, approximately 10%.
  • Legally authorised to work in the country where the position is based.

Beneficii

  • Base salary with performance-related incentives.
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Structured training and career development opportunities.

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