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(Senior) Manager Clinical Sciences(m/w/x)
Description
You will drive the development of novel cancer immunotherapies by designing clinical protocols and managing essential trial documentation in a collaborative, interdisciplinary environment.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
2 years
Tasks
- •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 & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Learning & Development
- •Conferences and trainings
Company Bike
- •Job bike
Public Transport Subsidies
- •Job ticket
Healthcare & Fitness
- •Health Programs
Childcare
- •Childcare benefits
Additional Allowances
- •Relocation allowance
Team Events
- •Company summer and winter events
- Immatics Biotechnologies GmbHFull-time/Part-timeWith HomeofficeManagementTübingen, München
- 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
(Senior) Manager Clinical Sciences(m/w/x)
The AI Job Search Engine
Description
You will drive the development of novel cancer immunotherapies by designing clinical protocols and managing essential trial documentation in a collaborative, interdisciplinary environment.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
2 years
Tasks
- •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 & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Learning & Development
- •Conferences and trainings
Company Bike
- •Job bike
Public Transport Subsidies
- •Job ticket
Healthcare & Fitness
- •Health Programs
Childcare
- •Childcare benefits
Additional Allowances
- •Relocation allowance
Team Events
- •Company summer and winter events
About the Company
Immatics
Industry
Pharmaceuticals
Description
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)
Full-time/Part-timeWith HomeofficeManagementTübingen, München - 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