Fortrea
Fortrea
Fortrea — биофармацевтикалық және медициналық технология компанияларына қызмет көрсететін жаһандық клиникалық зерттеу ұйымы. Оның клиникалық әзірлеу қызметтері клиникалық фармакологияны, I–IV фазалардағы зерттеулерді басқаруды, реттеуші стратегияны және нарыққа қолжетімділікті қамтып, ғылыми сараптаманы деректерге негізделген тәсілдермен ұштастырады. Fortrea жасушалық және гендік терапия, онкология, жүрек-қантамыр аурулары және жұқпалы ауруларды қоса алғанда, әртүрлі бағыттардағы бағдарламаларды қолдайды. Осы арқылы компания клиенттеріне әзірлеуге қатысты негізделген шешімдер қабылдауға және ықтимал емдеу әдістерін пациенттерге жеткізу үдерісін ілгерілетуге көмектеседі.

Clinical Research Associate, DACH (Germany Remote)

Monitor sponsor-dedicated clinical trial sites across Germany, Austria, and Switzerland. Support site selection, compliance, data quality, training, and regulatory activities for Fortrea.

Сипаттама

  • Identify and evaluate potential investigators and clinical trial sites
  • Recommend sites during feasibility and selection activities
  • Conduct pre-study, initiation, monitoring, and close-out visits
  • Track site performance, data quality, and protocol compliance
  • Serve as a primary contact for site staff, providing training and support
  • Apply data insights to evaluate risks and inform decisions
  • Support regulatory audits, ethics committee submissions, and system access coordination

Талаптар

  • Degree in life sciences, nursing, pharmacy, or a related allied health field; equivalent relevant experience may substitute for formal education
  • Basic to strong working knowledge of ICH/GCP guidelines and applicable clinical trial laws and regulations
  • Sound understanding of clinical research processes, regulations, and methodology
  • Strong organizational and time-management abilities
  • Ability to establish and maintain professional relationships
  • One to three years of monitoring experience in a CRO or pharmaceutical environment

Артықшылықтар

  • Regional monitoring model designed to reduce travel while maintaining impact
  • Supportive work environment
  • Opportunity to contribute to research intended to improve lives
  • Sponsor-dedicated team with a strong pipeline and clear purpose

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