IQVIA RDS GmbH
Local Trial Manager(m/w/x)
Vollzeit
mit Homeoffice
Senior
Keine Angabe
Frankfurt am Main
IQ
IQVIA RDS GmbH1 Monat
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Vollzeit
Remote
Berufserfahren
ab 70.100 / Jahr
Frankfurt am Main
Nejo KI-Zusammenfassung
As a Clinical Trial Manager, you will oversee the execution of clinical studies, ensuring compliance with regulations and ethical standards. Your role involves managing trial teams, coordinating with vendors, and maintaining strong relationships with investigational sites to drive successful trial outcomes.
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Anforderungen
- •Master’s or higher-level degree in life science
- •At least 2 years of clinical trial management experience
- •Significant exposure in managing Early Phase clinical trials
- •Exceptional knowledge of clinical research regulatory requirements
- •Excellent understanding of project financials and vendor management
- •Effective communication skills and fluent in German and English
- •High ability in abstract complex topics and strategic thinking
- •High organizational and planning skills
- •Excellent leadership and collaboration skills
- •High degree of self-accountability and commitment
- •Very good computer skills including Microsoft Word, Excel, PowerPoint
- •Flexibility for occasional business travel
- •Strong problem solving skills
- •Ability to make decisions and drive results
Master-Abschluss
Berufserfahrung
2 Jahre
Deine Aufgaben
- •Manage execution of clinical studies
- •Orchestrate local trial team activities
- •Integrate with other functions during trial phases
- •Work within GCP and regulatory environments
- •Collaborate with multidisciplinary international teams
- •Lead local trial team in preparing trial documents
- •Support investigative sites in contract and approval processes
- •Ensure compliance with ICH-GCP and regulatory regulations
- •Uphold ethical standards and patient safety
- •Plan and conduct trials in line with regulatory requirements
- •Set up and manage trial budgets
- •Review budget updates based on trial changes
- •Act as primary contact for vendors
- •Manage vendor-related activities as per project needs
- •Provide trial-specific training to internal and external partners
- •Develop relationships with investigational sites
- •Support CRAs in site communications
- •Monitor compliance of trial sites with GCP and regulations
- •Ensure adequate trial supply distribution to sites
- •Oversee timely data entry and cleaning
- •Facilitate on-time Data Base Lock
- •Collect and archive required trial documents
- •Identify risks and develop contingency plans
- •Collaborate with project leader on problem-solving
- •Report updates to Trial Leader
- •Participate in quality and process improvement initiatives
Tools & Technologien
Microsoft WordMicrosoft ExcelMicrosoft PowerPoint
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
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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