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Clinical Trial Coordinator II(m/w/x)
Description
You will drive clinical research excellence by managing regulatory documentation and site communications, ensuring every trial phase meets the highest standards of accuracy and compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in life sciences, equivalent education, training, or experience
- •Outstanding communication, teamwork, interpersonal, and time management skills
- •Excellent German (C1 level) and English languages
- •Same aptitude as other applicants (for severely disabled applicants)
Education
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 investigative sites
- •Resolve identified regulatory issues
- •Disseminate study information and project updates
- •Communicate with clients and clinical study teams
- •Identify potential investigators
- •Develop and distribute initial protocol packets
- •Prepare regulatory compliance review packages
- •Build meeting agendas and record minutes
- •Coordinate team conference calls
- •Adhere to Good Clinical Practices and regulations
- •Follow standard operating procedures for project execution
- •Analyze project data to ensure accuracy
- •Manage multiple projects with differing priorities
Languages
German – Business Fluent
English – Business Fluent
- Thermo Fisher ScientificFull-timeRemoteSeniorKarlsruhe, München
- HRA 11164 PPD Germany GmbH & Co KG
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Clinical Trial Coordinator II(m/w/x)
The AI Job Search Engine
Description
You will drive clinical research excellence by managing regulatory documentation and site communications, ensuring every trial phase meets the highest standards of accuracy and compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in life sciences, equivalent education, training, or experience
- •Outstanding communication, teamwork, interpersonal, and time management skills
- •Excellent German (C1 level) and English languages
- •Same aptitude as other applicants (for severely disabled applicants)
Education
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 investigative sites
- •Resolve identified regulatory issues
- •Disseminate study information and project updates
- •Communicate with clients and clinical study teams
- •Identify potential investigators
- •Develop and distribute initial protocol packets
- •Prepare regulatory compliance review packages
- •Build meeting agendas and record minutes
- •Coordinate team conference calls
- •Adhere to Good Clinical Practices and regulations
- •Follow standard operating procedures for project execution
- •Analyze project data to ensure accuracy
- •Manage multiple projects with differing priorities
Languages
German – Business Fluent
English – Business Fluent
About the Company
Thermo Fisher Scientific
Industry
Pharmaceuticals
Description
The company enables customers to make the world healthier, cleaner, and safer through innovative scientific solutions.
- Thermo Fisher Scientific
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