Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Full-time/Part-timeWith HomeofficeManagement
Tübingen, München
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IMImmatics
(Senior) Manager Clinical Sciences(m/w/x)
München
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
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
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
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GCP guidelines
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immatics and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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IMImmatics
(Senior) Manager Clinical Sciences(m/w/x)
München
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
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
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
Work Experience
- 2 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GCP guidelines
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Immatics and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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.
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