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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

Senior Clinical Trial Associate – Hybrid, Mannheim

Support clinical trial administration and operational delivery for ICON’s sponsor-dedicated pharmaceutical services. Coordinate regulatory documentation, site communications, trial records, and stakeholder activities.

DEGermaniaHibridNormă întreagăSeniorLimbă Obligatorie: germanăLimbă Obligatorie: englezăAsociat pentru studii cliniceGeneral

Descriere

  • Support clinical trials through documentation management, meeting coordination, and accurate maintenance of trial records
  • Prepare and submit regulatory documentation while maintaining alignment with study protocols and applicable requirements
  • Partner with cross-functional teams to advance trial operations and address issues arising during the study
  • Track study progress, coordinate site communications, and help ensure study materials are delivered on schedule
  • Develop effective working relationships with site personnel and other stakeholders to support efficient trial delivery
  • Own assigned clinical trial management deliverables and use specialist knowledge to address complex operational challenges

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Substantial experience supporting clinical trials, with a sound understanding of trial processes and regulatory requirements
  • Highly organized, able to prioritize and manage multiple tasks and projects effectively
  • Experience with clinical trial management systems and related software, with strong attention to documentation and data accuracy
  • Strong communication, interpersonal, and problem-solving abilities, along with the capacity to collaborate with varied teams and stakeholders
  • Willingness to travel as needed, approximately 10%
  • Fluency in German and English
  • Legal authorization 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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