IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Vollzeit
Remote
Berufserfahren
ab 70.100 / Jahr
Frankfurt am Main
IQ
IQVIA RDS GmbH1 Monat
Local Trial Manager(m/w/x)
Vollzeit
mit Homeoffice
Senior
Keine Angabe
Frankfurt am Main
Nejo KI-Zusammenfassung
As a Local Trial Manager, you will oversee clinical trials from home in Germany, ensuring compliance, managing budgets, and driving patient recruitment while collaborating with various teams to achieve research goals.
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Anforderungen
- •Master’s or higher-level degree in life science
- •Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO plus 1-3 years of local clinical trial management experience
- •Therapeutic area expertise in Oncology
- •Strong working knowledge of clinical research regulatory requirements, i.e., GCP and ICH guidelines
- •Fluent language skills in German on at least C1 level and good command of English
- •Strong IT skills in appropriate software and company systems
- •Excellent decision-making and strong financial management skills
- •Flexibility and ability to manage study teams in a virtual environment
- •Willingness to travel occasionally for business meetings
Master-Abschluss
Berufserfahrung
5 Jahre
Deine Aufgaben
- •Prepare high-level budget estimates for service requests
- •Develop detailed budget proposals
- •Manage contracts and review external service provider agreements
- •Act as the primary contact for assigned trials at the country level
- •Track project progress against planned timelines
- •Monitor patient recruitment rates to meet enrollment targets
- •Maintain and update trial management systems
- •Analyze trial progress using management reports
- •Participate in Health Authority inspections and internal audits
- •Contribute to site-level recruitment strategies and contingency plans
- •Manage vendor services and support vendor selection
- •Review country-specific informed consent documents
- •Ensure timely reporting of adverse events and serious adverse events
- •Maintain accurate trial data and essential documents
- •Collaborate with Global Trial Lead on quality issues
- •Ensure accurate financial reporting and budget adherence
- •Organize IEC/HA approvals to comply with local regulations
- •Mentor or represent the functional area in process initiatives
Tools & Technologien
GCPICH
Sprachen
Deutsch – verhandlungssicher
Englisch – fortgeschritten
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA RDS GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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