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Senior Clinical Trial Physician(m/w/x)
Description
In this role, you will provide essential medical leadership for clinical trials in hemato-oncology, ensuring compliance and safety while collaborating with diverse teams. Your expertise will shape study designs, regulatory submissions, and scientific publications.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree (MD) with valid license to practice
- •Board certification in hemato-oncology preferred
- •Strong medical and scientific background in hemato-oncology
- •Proven experience in clinical trial design, execution, and supervision
- •Experience with regulatory submissions (MAA/BLA) and scientific publications
- •Industry experience in Pharma/Biotech in global clinical development
- •Highly organized, detail-oriented, and proactive
- •Excellent communication and collaboration skills
- •Commitment to patient safety, regulatory compliance, and scientific integrity
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Provide medical leadership and scientific expertise
- •Plan and execute clinical trials in hemato-oncology
- •Contribute to study design and regulatory submissions
- •Review and analyze clinical trial data
- •Lead the design and implementation of clinical trial protocols
- •Ensure adherence to ICH-GCP and ethical standards
- •Supervise ongoing trials with Clinical Operations and Medical Monitors
- •Support protocol amendments as needed
- •Contribute to Clinical Study Reports and regulatory documentation
- •Develop scientific publications and presentations
- •Serve as a medical interface to internal and external stakeholders
- •Ensure regulatory compliance and provide medical guidance on safety
- •Collaborate with cross-functional teams for smooth execution of clinical programs
Languages
English – Business Fluent
Benefits
Flexible Working
- •Free and self-determined time management
- •Mobile working
Informal Culture
- •Intercultural environment
Purpose-Driven Work
- •Creative contribution freedom
Learning & Development
- •Individual further training
More Vacation Days
- •30 days of vacation
Corporate Discounts
- •Discounted ticket to Germany
Company Bike
- •(e)-bike leasing
Additional Allowances
- •Capital-forming benefits
Retirement Plans
- •Company pension plan
Other Benefits
- •Disability insurance
Free or Subsidized Food
- •Canteen
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Senior Clinical Trial Physician(m/w/x)
The AI Job Search Engine
Description
In this role, you will provide essential medical leadership for clinical trials in hemato-oncology, ensuring compliance and safety while collaborating with diverse teams. Your expertise will shape study designs, regulatory submissions, and scientific publications.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree (MD) with valid license to practice
- •Board certification in hemato-oncology preferred
- •Strong medical and scientific background in hemato-oncology
- •Proven experience in clinical trial design, execution, and supervision
- •Experience with regulatory submissions (MAA/BLA) and scientific publications
- •Industry experience in Pharma/Biotech in global clinical development
- •Highly organized, detail-oriented, and proactive
- •Excellent communication and collaboration skills
- •Commitment to patient safety, regulatory compliance, and scientific integrity
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Provide medical leadership and scientific expertise
- •Plan and execute clinical trials in hemato-oncology
- •Contribute to study design and regulatory submissions
- •Review and analyze clinical trial data
- •Lead the design and implementation of clinical trial protocols
- •Ensure adherence to ICH-GCP and ethical standards
- •Supervise ongoing trials with Clinical Operations and Medical Monitors
- •Support protocol amendments as needed
- •Contribute to Clinical Study Reports and regulatory documentation
- •Develop scientific publications and presentations
- •Serve as a medical interface to internal and external stakeholders
- •Ensure regulatory compliance and provide medical guidance on safety
- •Collaborate with cross-functional teams for smooth execution of clinical programs
Languages
English – Business Fluent
Benefits
Flexible Working
- •Free and self-determined time management
- •Mobile working
Informal Culture
- •Intercultural environment
Purpose-Driven Work
- •Creative contribution freedom
Learning & Development
- •Individual further training
More Vacation Days
- •30 days of vacation
Corporate Discounts
- •Discounted ticket to Germany
Company Bike
- •(e)-bike leasing
Additional Allowances
- •Capital-forming benefits
Retirement Plans
- •Company pension plan
Other Benefits
- •Disability insurance
Free or Subsidized Food
- •Canteen
About the Company
Miltenyi Biotec
Industry
Pharmaceuticals
Description
Das Unternehmen entwickelt einzigartige Lösungen für die biomedizinische Spitzenforschung sowie neuartige Zell- und Gentherapien.
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