Fisher Clinical Services GmbH
Project Support Associate - Distribution(m/w/x)
Vollzeitnur vor OrtJunior
Allschwil
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THThermo Fisher Scientific
Project Support Associate - Document writer(m/w/x)
VollzeitVor OrtJunior
Nejo KI-Zusammenfassung
Managing clinical trial documentation and coordinating supply chain activities for a global health solutions provider. Bachelor's degree in clinical trials or pharmaceutical industry required. Work with internal teams and clients on project planning and documentation management.
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Anforderungen
- Adherence to GMP and safety standards
- Bachelor's degree in clinical trials or pharmaceutical industry
- Preferred study fields: healthcare, supply chain, life sciences
- Strong understanding of GMP/GxP principles and quality systems
- Project management skills, handling multiple projects
- Advanced Microsoft Office proficiency (Excel, Project)
- Strong analytical and problem-solving capabilities
- Effective written and verbal communication skills
- Detail-oriented with excellent organization and documentation
- Ability to work independently and in cross-functional teams
- Fluent English required, additional languages beneficial
- Experience coordinating teams and managing stakeholders
- Ability to analyze data and generate reports
- Focus on quality service and continuous improvement
- Adaptable to changing priorities with attention to detail
Aufgaben
- Support clinical trials by managing project documentation
- Coordinate supply chain activities
- Ensure consistent delivery of services
- Work closely with internal teams and clients
- Handle project planning and documentation management
- Maintain cross-functional coordination to meet timelines
- Monitor daily progress of client project results
- Maintain accurate records for all work undertaken
- Collaborate with the Project Manager to meet customer and study requirements
- Use project planning tools to communicate achievements and critical path activities
- Create and support creation of operational documentation
- Build bill of materials
- Coordinate creation and review of billing packages
- Collect information on study design
- Coordinate primary and secondary packaging materials
- Coordinate label translation
- Produce batch documentation for operations
- Check documentation and GMP instructions
- Apply GXP in all areas of responsibility
- Understand project plans and timeline management
- Deliver tasks to achieve goals
- Identify and raise project challenges
- Collaborate with team members to resolve issues
- Communicate information in a timely manner
- Respect differences and address challenging situations appropriately
Ausbildung
Bachelor-Abschluss
Sprachen
Englisch – fließend
Tools & Technologien
Microsoft OfficeExcelProject
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Nejo hat diesen Job automatisch von der Website des Unternehmens Thermo Fisher Scientific 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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TH
HealthcareAllschwil
The company enables customers to make the world healthier, cleaner, and safer through innovative scientific solutions.
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