Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Full-time/Part-timeWith HomeofficeExperienced
Tübingen, München
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IM
Immatics Biotechnologies GmbHMedical Monitor*(m/w/x)
Tübingen, München, Berlin
Full-time, Part-timeWith Home OfficeExperienced
Description
You will drive clinical trial success by providing expert medical oversight and safety analysis. From protocol design to regulatory filings, you'll ensure patient safety and data integrity.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical doctor degree
- •Prior experience as Medical Monitor
- •Experience in oncology and cell therapy
- •Experience in clinical development or trial oversight
- •High degree of independent working
- •Attention to detail
- •Problem solving skills
- •Very good English communication skills
- •German language skills as a plus
Education
Doctoral / PhD
Tasks
- •Provide medical oversight for Phase 1 to 3 clinical trials
- •Assess adverse events for causality and clinical management
- •Review CIOMS and MedWatch safety forms
- •Serve as the primary contact for medical investigator inquiries
- •Review medical plans and safety data documents
- •Lead medical data review and DSMB meetings
- •Collaborate with Drug Safety on signal detection
- •Provide medical input for trial design and protocols
- •Review and approve electronic Case Report Forms
- •Develop content for Investigator Brochures
- •Ensure protocol compliance for dosing and safety assessments
- •Participate in protocol deviation assessments
- •Support site selection and staff training
- •Contribute to investigator meetings and site visits
- •Support regulatory filings and risk management plans
- •Perform medical reviews of safety and efficacy data
- •Review patient narratives and interpret clinical data
- •Contribute to study reports, publications, and presentations
Languages
English – Business Fluent
German – Basic
Benefits
Learning & Development
- •Conferences and trainings
Company Bike
- •Job bike
Public Transport Subsidies
- •Job ticket
Healthcare & Fitness
- •Health Programs
Childcare
- •Childcare benefits
Additional Allowances
- •Relocation allowance
Team Events
- •Company summer and winter events
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immatics Biotechnologies GmbH 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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IM
Immatics Biotechnologies GmbHMedical Monitor*(m/w/x)
Tübingen, München, Berlin
Full-time, Part-timeWith Home OfficeExperienced
New Job?Nejo!
The AI Job Search Engine
Description
You will drive clinical trial success by providing expert medical oversight and safety analysis. From protocol design to regulatory filings, you'll ensure patient safety and data integrity.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical doctor degree
- •Prior experience as Medical Monitor
- •Experience in oncology and cell therapy
- •Experience in clinical development or trial oversight
- •High degree of independent working
- •Attention to detail
- •Problem solving skills
- •Very good English communication skills
- •German language skills as a plus
Education
Doctoral / PhD
Tasks
- •Provide medical oversight for Phase 1 to 3 clinical trials
- •Assess adverse events for causality and clinical management
- •Review CIOMS and MedWatch safety forms
- •Serve as the primary contact for medical investigator inquiries
- •Review medical plans and safety data documents
- •Lead medical data review and DSMB meetings
- •Collaborate with Drug Safety on signal detection
- •Provide medical input for trial design and protocols
- •Review and approve electronic Case Report Forms
- •Develop content for Investigator Brochures
- •Ensure protocol compliance for dosing and safety assessments
- •Participate in protocol deviation assessments
- •Support site selection and staff training
- •Contribute to investigator meetings and site visits
- •Support regulatory filings and risk management plans
- •Perform medical reviews of safety and efficacy data
- •Review patient narratives and interpret clinical data
- •Contribute to study reports, publications, and presentations
Languages
English – Business Fluent
German – Basic
Benefits
Learning & Development
- •Conferences and trainings
Company Bike
- •Job bike
Public Transport Subsidies
- •Job ticket
Healthcare & Fitness
- •Health Programs
Childcare
- •Childcare benefits
Additional Allowances
- •Relocation allowance
Team Events
- •Company summer and winter events
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immatics Biotechnologies GmbH 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.
About the Company
Immatics Biotechnologies GmbH
Industry
Pharmaceuticals
Description
The company combines the discovery of true targets for cancer immunotherapies with the development of T cell receptors to enable robust T cell responses against cancer.
Not a perfect match?
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Full-time/Part-timeWith HomeofficeSeniorTübingen, München - Immatics Biotechnologies GmbH
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