PPD Germany GmbH & Co KG
Clinical Trial Coordinator - FSP(m/w/x)
Full-timeWith HomeofficeNot specified
Karlsruhe
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THThermo Fisher Scientific
Clinical Trial Coordinator II(m/w/x)
Karlsruhe
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Thermo Fisher Scientific and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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THThermo Fisher Scientific
Clinical Trial Coordinator II(m/w/x)
Karlsruhe
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Thermo Fisher Scientific and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Thermo Fisher Scientific
Industry
Healthcare
Description
The company enables customers to make the world healthier, cleaner, and safer through innovative scientific solutions.
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