Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Full-time/Part-timeWith HomeofficeExperienced
Tübingen, München, Berlin
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IMImmatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Tübingen, München
Full-time, Part-timeWith Home OfficeExperienced
Nejo AI Summary
Medical oversight for Phase 1-3 clinical trials assessing adverse events in cancer immunotherapy. MD PhD in Biomedical Sciences, prior Medical Monitor experience, and oncology/cell therapy background required. Job bike, job ticket, childcare benefits, and relocation allowance.
Requirements
- MD PhD in Biomedical Sciences or related field
- Prior experience as a Medical Monitor
- Experience in oncology and cell therapy
- High degree of independent working
- Attention to detail
- Problem solving skills
- Very good communication skills in English
- German language skills are a plus
Tasks
- Provide medical oversight for clinical trials from Phase 1 to Phase 3
- Assess (Serious) Adverse Events for causality, expectedness, and clinical management
- Serve as the primary contact for medical investigator inquiries
- Review safety data documents and related materials
- Lead and support medical data review meetings and DSMB meetings
- Collaborate with Drug Safety on signal detection
- Provide medical input on trial design and protocol development
- Review and approve electronic Case Report Forms (eCRFs)
- Contribute to Investigator Brochures
- Ensure compliance with eligibility criteria and safety assessments
- Participate in protocol deviation assessments
- Support investigators with protocol-related questions
- Participate in site selection and training activities
- Contribute to Investigator Meetings and site visits as needed
- Support regulatory filings and respond to regulatory inquiries
- Provide medical expertise for Risk Management Plans
- Ensure timely medical review of safety and efficacy data
- Review patient narratives
- Contribute to data interpretation in early clinical trials
- Assist in clinical study reports, publications, and presentations
Work Experience
- approx. 1 - 4 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
- German – Basic
Benefits
Company Bike
- Job bike
Public Transport Subsidies
- Job ticket
Healthcare & Fitness
- Health programs
Childcare
- Childcare benefits
Additional Allowances
- Relocation allowance
Team Events
- Company summer events
- Company 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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IMImmatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Tübingen, München
Full-time, Part-timeWith Home OfficeExperienced
Nejo AI Summary
Medical oversight for Phase 1-3 clinical trials assessing adverse events in cancer immunotherapy. MD PhD in Biomedical Sciences, prior Medical Monitor experience, and oncology/cell therapy background required. Job bike, job ticket, childcare benefits, and relocation allowance.
Requirements
- MD PhD in Biomedical Sciences or related field
- Prior experience as a Medical Monitor
- Experience in oncology and cell therapy
- High degree of independent working
- Attention to detail
- Problem solving skills
- Very good communication skills in English
- German language skills are a plus
Tasks
- Provide medical oversight for clinical trials from Phase 1 to Phase 3
- Assess (Serious) Adverse Events for causality, expectedness, and clinical management
- Serve as the primary contact for medical investigator inquiries
- Review safety data documents and related materials
- Lead and support medical data review meetings and DSMB meetings
- Collaborate with Drug Safety on signal detection
- Provide medical input on trial design and protocol development
- Review and approve electronic Case Report Forms (eCRFs)
- Contribute to Investigator Brochures
- Ensure compliance with eligibility criteria and safety assessments
- Participate in protocol deviation assessments
- Support investigators with protocol-related questions
- Participate in site selection and training activities
- Contribute to Investigator Meetings and site visits as needed
- Support regulatory filings and respond to regulatory inquiries
- Provide medical expertise for Risk Management Plans
- Ensure timely medical review of safety and efficacy data
- Review patient narratives
- Contribute to data interpretation in early clinical trials
- Assist in clinical study reports, publications, and presentations
Work Experience
- approx. 1 - 4 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
- German – Basic
Benefits
Company Bike
- Job bike
Public Transport Subsidies
- Job ticket
Healthcare & Fitness
- Health programs
Childcare
- Childcare benefits
Additional Allowances
- Relocation allowance
Team Events
- Company summer events
- Company 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Immatics Biotechnologies GmbH
Industry
Healthcare
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.
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