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
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
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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