Dein persönlicher KI-Karriere-Agent
Clinical Trial Coordinator II(m/w/x)
Regulatory document review and issue resolution with monitors and sites for clinical research. GCP and clinical regulations adherence, with multi-project management experience required. Project tracking tools utilized for issue management.
Anforderungen
- Degree in life sciences or equivalent
- Adherence to GCP and clinical regulations
- Ability to analyze project data accurately
- Experience managing multiple simultaneous projects
- Outstanding communication and teamwork skills
- Excellent interpersonal and time management
- Excellent English and German skills
Aufgaben
- Review investigator files for clinical research services
- Log outstanding issues in project tracking tools
- Review regulatory documents for proper content
- Liaise with monitors and sites to resolve regulatory issues
- Disseminate study information and tracking updates to stakeholders
- Identify potential investigators and distribute protocol packets
- Prepare regulatory compliance review packages
- Build meeting agendas and record minutes
- Coordinate team conference calls and distribute minutes
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
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Clinical Trial Coordinator II(m/w/x)
Regulatory document review and issue resolution with monitors and sites for clinical research. GCP and clinical regulations adherence, with multi-project management experience required. Project tracking tools utilized for issue management.
Anforderungen
- Degree in life sciences or equivalent
- Adherence to GCP and clinical regulations
- Ability to analyze project data accurately
- Experience managing multiple simultaneous projects
- Outstanding communication and teamwork skills
- Excellent interpersonal and time management
- Excellent English and German skills
Aufgaben
- Review investigator files for clinical research services
- Log outstanding issues in project tracking tools
- Review regulatory documents for proper content
- Liaise with monitors and sites to resolve regulatory issues
- Disseminate study information and tracking updates to stakeholders
- Identify potential investigators and distribute protocol packets
- Prepare regulatory compliance review packages
- Build meeting agendas and record minutes
- Coordinate team conference calls and distribute minutes
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Über das Unternehmen
Thermo Fisher Scientific
Branche
Healthcare
Beschreibung
The company enables customers to make the world healthier, cleaner, and safer through innovative scientific solutions.
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