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Project Manager Pre-Clinical Studies(m/w/x)
Description
You will drive the success of veterinary research by leading multidisciplinary teams and advising clients on study design while ensuring all pre-clinical trials meet strict global quality standards.
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 veterinary medicine, animal science, life sciences, or related field
- •Master’s degree or specialized training in clinical studies management or monitoring (asset)
- •Prior experience in clinical study monitoring environment (asset)
- •Ability to learn new tasks and knowledge areas
- •Independent and structured way of working
- •Reliability and high sense of responsibility
- •Excellent command of written and spoken English
- •Additional foreign language skills (asset)
- •Good teamwork and communication skills
- •Willingness to travel for business
- •Driver‘s license class B
Education
Tasks
- •Comply with VICH GCP and GLP regulatory requirements
- •Advise clients on international study design and placement
- •Lead multidisciplinary teams and train study investigators
- •Monitor study activities and conduct site visits
- •Track study cases, adverse events, and protocol compliance
- •Supervise laboratory diagnostics and drug accountability
- •Manage study site finances and approve invoices
- •Perform continuous quality control on collected study data
- •Prepare and review study protocols and final reports
- •Manage project budgets and report to middle management
Languages
English – Business Fluent
Benefits
Other Benefits
- •Detailed introduction to work
Diverse Work
- •Challenging field of activity
Informal Culture
- •International team
- •Positive and collegial atmosphere
Family Support
- •Family-friendly environment
Learning & Development
- •Continuous education options
- KLIFOVET GmbHFull-timeOn-siteExperiencedMünchen
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Project Manager Pre-Clinical Studies(m/w/x)
The AI Job Search Engine
Description
You will drive the success of veterinary research by leading multidisciplinary teams and advising clients on study design while ensuring all pre-clinical trials meet strict global quality standards.
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 veterinary medicine, animal science, life sciences, or related field
- •Master’s degree or specialized training in clinical studies management or monitoring (asset)
- •Prior experience in clinical study monitoring environment (asset)
- •Ability to learn new tasks and knowledge areas
- •Independent and structured way of working
- •Reliability and high sense of responsibility
- •Excellent command of written and spoken English
- •Additional foreign language skills (asset)
- •Good teamwork and communication skills
- •Willingness to travel for business
- •Driver‘s license class B
Education
Tasks
- •Comply with VICH GCP and GLP regulatory requirements
- •Advise clients on international study design and placement
- •Lead multidisciplinary teams and train study investigators
- •Monitor study activities and conduct site visits
- •Track study cases, adverse events, and protocol compliance
- •Supervise laboratory diagnostics and drug accountability
- •Manage study site finances and approve invoices
- •Perform continuous quality control on collected study data
- •Prepare and review study protocols and final reports
- •Manage project budgets and report to middle management
Languages
English – Business Fluent
Benefits
Other Benefits
- •Detailed introduction to work
Diverse Work
- •Challenging field of activity
Informal Culture
- •International team
- •Positive and collegial atmosphere
Family Support
- •Family-friendly environment
Learning & Development
- •Continuous education options
About the Company
Argenta
Industry
Pharmaceuticals
Description
Argenta is a leading global CRO and CDMO focused exclusively on animal health, providing support for product development and regulatory approval.
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