ICON plc
ICON plc
ICON plc ir globāla līgumizpētes organizācija, kas apkalpo veselības aprūpes un farmācijas nozares. Tās darbība ietver klīniskos, konsultāciju un komerciālos pakalpojumus, kas atbalsta zāļu izstrādi no agrīnas izpētes līdz darbībām pēc zāļu nonākšanas tirgū. Uzņēmums piedāvā decentralizētus klīniskos pētījumus, sirds drošuma novērtēšanu, agrīnās klīniskās laboratorijas pakalpojumus, medicīnisko attēlveidošanu, regulatīvo informāciju un reālās pasaules pierādījumu risinājumus. ICON plc ir arī terapeitiskā kompetence tādās jomās kā sirds un asinsvadu slimības, onkoloģija, iekšķīgās slimības, šūnu un gēnu terapijas, kā arī bioloģiski līdzīgas zāles. Apvienojot datu analīzi ar uz pacientu vērstām pieejām, uzņēmums palīdz attīstīt klīniskās programmas.

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.

Apraksts

  • 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

Prasības

  • 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

Priekšrocības

  • 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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