As an intern in Clinical Project Management / Clinical Monitoring you will gain practical insights into the operational side of clinical studies and support our team in a variety of organizational and documentationrelated tasks. Your responsibilities include:
- Supporting Trial Master File (TMF) activities
Helping with TMF planning document handling and simple reconciliation tasks to ensure study documentation is complete - Preparing EndNote libraries
Assisting with organizing and maintaining reference libraries for clinical documents - Supporting the creation of functional plans
Helping draft and structure operational plans used across clinical projects - Assisting with TFL reviews
Supporting the team in reviewing tables figures and listings to ensure accuracy and consistency - Helping maintain trackers
Working with CPMs/CTMs and other functions (e.g. labs) to set up or update studyrelated tracking tools - Supporting contract and vendor management tasks
Assisting with general oversight activities and coordinationnot limited to studyspecific tasks - Preparing Master ISF and Site ISF documents
Helping organize essential study materials for investigational sites - Providing support to CRAs
Sharing EDC listings and query reports to help monitor study progress
Qualifications :
- You are an enrolled student in life sciences health sciences or a datarelated field.
- Interest in clinical research and working with data
- Careful detailoriented working style
- Willingness to learn new software tools
- Good English and German skills
- Reliable proactive mindset
- Your workplace will be Bergisch Gladbach.
Additional Information :
The internship can be voluntary or mandatory - as you require.
What we offer
- A modern workplace in Bergisch Gladbach with opportunity for some mobile work. Exciting opportunities in the development of technologies with a secure future.
- Cross-border intercultural cooperation and short communication channels
- A collegial corporate culture and flexible working hours enable time management on your own terms
- Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University
- Diverse corporate benefits with regard to employee health sport and staff events
We look forward to your application
If you want to work in an open creative and supportive team this is the place for you. We look forward to receiving your application along with your salary expectations and availability.
Remote Work :
No
Employment Type :
Full-time
As an intern in Clinical Project Management / Clinical Monitoring you will gain practical insights into the operational side of clinical studies and support our team in a variety of organizational and documentationrelated tasks. Your responsibilities include:Supporting Trial Master File (TMF) activi...
As an intern in Clinical Project Management / Clinical Monitoring you will gain practical insights into the operational side of clinical studies and support our team in a variety of organizational and documentationrelated tasks. Your responsibilities include:
- Supporting Trial Master File (TMF) activities
Helping with TMF planning document handling and simple reconciliation tasks to ensure study documentation is complete - Preparing EndNote libraries
Assisting with organizing and maintaining reference libraries for clinical documents - Supporting the creation of functional plans
Helping draft and structure operational plans used across clinical projects - Assisting with TFL reviews
Supporting the team in reviewing tables figures and listings to ensure accuracy and consistency - Helping maintain trackers
Working with CPMs/CTMs and other functions (e.g. labs) to set up or update studyrelated tracking tools - Supporting contract and vendor management tasks
Assisting with general oversight activities and coordinationnot limited to studyspecific tasks - Preparing Master ISF and Site ISF documents
Helping organize essential study materials for investigational sites - Providing support to CRAs
Sharing EDC listings and query reports to help monitor study progress
Qualifications :
- You are an enrolled student in life sciences health sciences or a datarelated field.
- Interest in clinical research and working with data
- Careful detailoriented working style
- Willingness to learn new software tools
- Good English and German skills
- Reliable proactive mindset
- Your workplace will be Bergisch Gladbach.
Additional Information :
The internship can be voluntary or mandatory - as you require.
What we offer
- A modern workplace in Bergisch Gladbach with opportunity for some mobile work. Exciting opportunities in the development of technologies with a secure future.
- Cross-border intercultural cooperation and short communication channels
- A collegial corporate culture and flexible working hours enable time management on your own terms
- Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University
- Diverse corporate benefits with regard to employee health sport and staff events
We look forward to your application
If you want to work in an open creative and supportive team this is the place for you. We look forward to receiving your application along with your salary expectations and availability.
Remote Work :
No
Employment Type :
Full-time
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