ClinTec Austria GmbH

Qualifications: Degree in Market Research, Psychology, Economics, Statistics, Business, Life Sciences, Public Health, or a related discipline. Minimum 5 years of experience in primary market research, healthcare market research, consumer insights, consulting research, management consulting, or a related function. Strong expertise in quantitative and/or qualitative research methodologies. Proven experience designing surveys and managing end-to-end research studies, including overseeing questionnaire programming, testing, and quality control – also in collaboration with external vendors. Ability to manage multiple projects simultaneously in a fast-paced environment. Strong analytical mindset with the ability to synthesize data into actionable recommendations – with experience in modern ...

Aufgaben Als Clinical Research Coordinator unterstützen Sie das Studienteam vor Ort bei der Durchführung der klinischen Studie. Zu Ihren Aufgaben können unter anderem gehören: Unterstützung bei der Organisation und Koordination des Studienablaufs Betreuung von Studienpatient:innen im Rahmen der vorgesehenen Studienvisiten Vorbereitung und Koordination von Patientenvisiten Unterstützung bei studienbezogener Dokumentation und Datenerfassung Pflege und Aktualisierung der Studiendokumentation Zusammenarbeit mit Prüfärzt:innen und weiteren Mitgliedern des Studienteams Unterstützung bei administrativen und organisatorischen Aufgaben rund um die klinische Studie Sicherstellung eines strukturierten und reibungslosen Studienablaufs am Prüfzentrum Ihr Profil Abgeschlossene Ausbildung im ...

requirements into clear actions, ownership, priorities and realistic timelines for the core and extended team. Oversee delivery partners: Maintain effective oversight of clinical Phase I units, CROs, laboratories, vendors and outsourced services, including scope, performance, quality, dependencies, financials and issue resolution in collaboration with accountable functions. Maintain quality and compliance: Ensure adherence to GCP, ICH, applicable global and local regulations, sponsor procedures and inspection-ready documentation throughout the trial lifecycle. Ensure consistent use of study tools, training materials and standard processes. Use data to steer performance: Use study systems, dashboards, metrics and operational reviews to monitor study progress, safety and data flows, ...

requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. Effective communication, organizational and planning skills. Ability to work independently and to effectively prioritize tasks while working on multiple projects. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Flexibility to visit our client's office within the Vienna region on a regular basis. Monthly gross salary: starting at 3.000 EUR basic - an overpay according to skills and working experience is possible. Please apply with your English CV and ...