Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahren
Tübingen, München, Berlin
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
IMImmatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Tübingen, München
Vollzeit, Teilzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Benefits
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer events
- Company winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics Biotechnologies GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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IMImmatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Tübingen, München
Vollzeit, Teilzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Benefits
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer events
- Company winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics Biotechnologies GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Immatics Biotechnologies GmbH
Branche
Healthcare
Beschreibung
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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