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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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Locurile de muncă ale companiei

Clinical Associate - Poland (Remote)

Support sponsor-dedicated clinical trials for ICON Strategic Solutions in Poland by coordinating study activities, documentation, monitoring, and close-out.

PLPoloniaRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăAsociatGeneral

Descriere

  • Support clinical trial planning, execution, and monitoring
  • Maintain compliance with protocols, regulations, and industry standards
  • Coordinate site initiation, patient recruitment, data collection, and monitoring visits
  • Maintain accurate and timely study data and documentation
  • Partner with Clinical Operations, Data Management, and Biometrics teams
  • Keep complete and organized study records
  • Follow applicable regulations and standard operating procedures
  • Support close-out through data cleaning, analysis, and clinical study report preparation

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare-related field
  • At least two years of experience as a Clinical Trial Assistant
  • Prior clinical research or healthcare experience, preferably in pharmaceuticals, biotechnology, or contract research
  • Experience with trial master files and other clinical trial technologies
  • Strong organizational and time-management skills
  • Ability to prioritize work and manage competing demands
  • Excellent attention to detail and problem-solving skills
  • Commitment to data accuracy, integrity, and compliance
  • Effective communication and interpersonal skills
  • Ability to work cross-functionally and build strong relationships with study teams and clinical sites
  • Willingness to travel approximately 60% as required
  • Legal right to work in Poland

Beneficii

  • Competitive base salary with performance-based 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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