Die KI-Suchmaschine für Jobs
(Senior) Manager Clinical Sciences(m/w/x)
Beschreibung
You will drive the development of novel cancer immunotherapies by designing clinical protocols and managing essential trial documentation in a collaborative, interdisciplinary environment.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
2 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
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
- Immatics Biotechnologies GmbHVollzeit/Teilzeitmit HomeofficeManagementTübingen, München
- Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
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)
Vollzeit/Teilzeitmit HomeofficeSeniorTübingen, München
(Senior) Manager Clinical Sciences(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You will drive the development of novel cancer immunotherapies by designing clinical protocols and managing essential trial documentation in a collaborative, interdisciplinary environment.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
2 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
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
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.
- Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagementTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
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)
Vollzeit/Teilzeitmit HomeofficeSeniorTübingen, München