The AI Job Search Engine
Director Clinical Sciences(m/w/x)
Clinical development of T cell receptor cancer immunotherapies, leading cross-functional teams for regulatory submissions. Master's/PhD in Life Sciences and 7 years clinical trial conduct experience required. Job bike, job ticket, childcare benefits, relocation allowance.
Requirements
- Master’s degree or PhD in Biology, Clinical Sciences, or Life Sciences
- Minimum of 7 years’ experience in clinical trial conduct
- Comprehensive knowledge of Good Clinical Practice (GCP)
- Strong understanding of clinical development processes
- Proven ability to lead cross-functional teams
- Excellent verbal and written communication skills in English and German
- Ability to work independently while collaborating effectively
- Demonstrated flexibility and adaptability in dynamic environments
- Proactive mindset combined with a structured approach to work
Tasks
- Drive clinical development of cancer immunotherapies
- Lead and oversee (Senior) Managers Clinical Sciences
- Provide strategic input for advisory boards and KOL interactions
- Lead cross-functional teams for regulatory submissions
- Author and manage clinical trial protocols and related documents
- Prepare and review clinical sections of briefing books
- Prepare and review clinical sections of investigator brochures
- Conduct trainings for clinical sites and internal teams
- Establish functional plans for controlled document compliance
- Manage internal and external stakeholders
- Organize data review meetings for clinical trial analysis
- Provide subject matter expertise in clinical research programs
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
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
Not a perfect match?
- Immatics Biotechnologies GmbHFull-time/Part-timeWith HomeofficeExperiencedTübingen, München
- Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedTübingen, München, Berlin - Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Full-timeWith HomeofficeExperiencedTübingen, München - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorTübingen, München - Philips
Medical&Clinical Affairs PMO&Transformation Manager(m/w/x)
Full-timeWith HomeofficeSeniorBöblingen
Director Clinical Sciences(m/w/x)
Clinical development of T cell receptor cancer immunotherapies, leading cross-functional teams for regulatory submissions. Master's/PhD in Life Sciences and 7 years clinical trial conduct experience required. Job bike, job ticket, childcare benefits, relocation allowance.
Requirements
- Master’s degree or PhD in Biology, Clinical Sciences, or Life Sciences
- Minimum of 7 years’ experience in clinical trial conduct
- Comprehensive knowledge of Good Clinical Practice (GCP)
- Strong understanding of clinical development processes
- Proven ability to lead cross-functional teams
- Excellent verbal and written communication skills in English and German
- Ability to work independently while collaborating effectively
- Demonstrated flexibility and adaptability in dynamic environments
- Proactive mindset combined with a structured approach to work
Tasks
- Drive clinical development of cancer immunotherapies
- Lead and oversee (Senior) Managers Clinical Sciences
- Provide strategic input for advisory boards and KOL interactions
- Lead cross-functional teams for regulatory submissions
- Author and manage clinical trial protocols and related documents
- Prepare and review clinical sections of briefing books
- Prepare and review clinical sections of investigator brochures
- Conduct trainings for clinical sites and internal teams
- Establish functional plans for controlled document compliance
- Manage internal and external stakeholders
- Organize data review meetings for clinical trial analysis
- Provide subject matter expertise in clinical research programs
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
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
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.
Not a perfect match?
- Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedTübingen, München, Berlin - Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Full-timeWith HomeofficeExperiencedTübingen, München - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorTübingen, München - Philips
Medical&Clinical Affairs PMO&Transformation Manager(m/w/x)
Full-timeWith HomeofficeSeniorBöblingen