Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagement
Tübingen, München
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IMImmatics
(Senior) Manager Clinical Sciences(m/w/x)
München
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Developing clinical trial protocols and designing EDC databases for novel PRAME immunotherapies at biotech firm focused on T cell receptor development. Experience with early/late-phase oncological trials and solid GCP knowledge required. Job bike, job ticket, childcare benefits.
Anforderungen
- University degree in Biology, Clinical/Life Sciences, or related field
- At least 2 years of professional experience in Clinical Trials
- Solid knowledge of GCP guidelines
- Deep understanding of Clinical Development processes
- Experience with early-/late-phase or pivotal oncological trials
- Interest in oncology clinical research and patient safety
- Ambition to make a difference for cancer patients
- Teamwork and excellent collaboration skills
- Ability to inspire colleagues
- Outstanding communication skills in English
- German language skills (advantageous)
- Openness and creativity regarding changing requirements
- Ability to think outside the box
- High level of flexibility
- Structured and reliable working style
- Strong analytical thinking
Aufgaben
- Develop clinical trial protocols and concept sheets
- Participate in scientific and procedural trial design discussions
- Prepare trial manuals and investigator meeting materials
- Develop patient information sheets and informed consent forms
- Design and develop electronic data capture databases
- Address protocol-related questions from stakeholders and investigators
- Perform patient profile reviews under medical supervision
- Review data listings, summary tables, and clinical reports
- Prepare manuscripts and scientific presentations
- Assist in the preparation of regulatory documents
- Summarize and interpret scientific information from published literature
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- GCP guidelines
Benefits
Weiterbildungsangebote
- Conferences and trainings
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health Programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer and winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics 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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(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
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IMImmatics
(Senior) Manager Clinical Sciences(m/w/x)
München
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Developing clinical trial protocols and designing EDC databases for novel PRAME immunotherapies at biotech firm focused on T cell receptor development. Experience with early/late-phase oncological trials and solid GCP knowledge required. Job bike, job ticket, childcare benefits.
Anforderungen
- University degree in Biology, Clinical/Life Sciences, or related field
- At least 2 years of professional experience in Clinical Trials
- Solid knowledge of GCP guidelines
- Deep understanding of Clinical Development processes
- Experience with early-/late-phase or pivotal oncological trials
- Interest in oncology clinical research and patient safety
- Ambition to make a difference for cancer patients
- Teamwork and excellent collaboration skills
- Ability to inspire colleagues
- Outstanding communication skills in English
- German language skills (advantageous)
- Openness and creativity regarding changing requirements
- Ability to think outside the box
- High level of flexibility
- Structured and reliable working style
- Strong analytical thinking
Aufgaben
- Develop clinical trial protocols and concept sheets
- Participate in scientific and procedural trial design discussions
- Prepare trial manuals and investigator meeting materials
- Develop patient information sheets and informed consent forms
- Design and develop electronic data capture databases
- Address protocol-related questions from stakeholders and investigators
- Perform patient profile reviews under medical supervision
- Review data listings, summary tables, and clinical reports
- Prepare manuscripts and scientific presentations
- Assist in the preparation of regulatory documents
- Summarize and interpret scientific information from published literature
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- GCP guidelines
Benefits
Weiterbildungsangebote
- Conferences and trainings
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health Programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer and winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics 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.
Über das Unternehmen
Immatics
Branche
Pharmaceuticals
Beschreibung
Immatics combines target discovery with T cell receptor development for cancer immunotherapies, aiming to deliver novel PRAME immunotherapies to patients with cancer.
Noch nicht perfekt?
- Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagementTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
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Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
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