AOP Health
Manager Medical Information(m/w/x)
Full-timeWith HomeofficeSenior
Wien
from 45,080 / year
New Job?Nejo!
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BOBoehringer Ingelheim
Study Physician(m/w/x)
Wien
from 108,000 / year
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Medical oversight of clinical trial protocols and data review for global pharmaceutical research. Specialization in Internal Medicine or General Practice with industry experience required. Additional bridge-days off and subsidized staff restaurant.
Requirements
- Medical degree with clinical training
- At least 4 years clinical practice
- Specialization in Internal Medicine or General Practice
- Experience in pharmaceutical industry or CRO
- Understanding of ICH-GCP and clinical research
- Strong analytical and communication skills
- Structured working style and international collaboration
- Proficiency in medical data review
- Fluency in English
Tasks
- Provide end-to-end medical support throughout the study lifecycle
- Ensure high-quality medical content in clinical trial protocols
- Collaborate with cross-functional stakeholders on trial development
- Develop the Clinical Quality Monitoring Plan
- Conduct ongoing medical data reviews
- Support risk-based quality management
- Define key protocol deviations
- Provide medical input for investigator and team trainings
- Advise on eCRF design and automated data checks
- Review ICFs, lab alerts, and recruitment activities
- Contribute to regulatory and ethics committee responses
- Address medical questions from investigators
- Support adjudication and Data Monitoring Committee processes
- Provide state-of-the-art medical expertise to project teams
- Execute medical oversight during trial preparation and conduct
- Manage medical reporting for clinical trials
- Serve as a core member of the Trial Team
- Participate in the Evidence Network for the asset
Work Experience
- 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- ICH-GCP regulations
Benefits
Flexible Working
- Home office
- Flexible working hours
- Flexible working time models
More Vacation Days
- Additional bridge-days off
Free or Subsidized Food
- Subsidized staff restaurant
- Subsidized cafeteria
- Vegetarian and vegan options
Learning & Development
- Learning and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim 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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BOBoehringer Ingelheim
Study Physician(m/w/x)
Wien
from 108,000 / year
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Medical oversight of clinical trial protocols and data review for global pharmaceutical research. Specialization in Internal Medicine or General Practice with industry experience required. Additional bridge-days off and subsidized staff restaurant.
Requirements
- Medical degree with clinical training
- At least 4 years clinical practice
- Specialization in Internal Medicine or General Practice
- Experience in pharmaceutical industry or CRO
- Understanding of ICH-GCP and clinical research
- Strong analytical and communication skills
- Structured working style and international collaboration
- Proficiency in medical data review
- Fluency in English
Tasks
- Provide end-to-end medical support throughout the study lifecycle
- Ensure high-quality medical content in clinical trial protocols
- Collaborate with cross-functional stakeholders on trial development
- Develop the Clinical Quality Monitoring Plan
- Conduct ongoing medical data reviews
- Support risk-based quality management
- Define key protocol deviations
- Provide medical input for investigator and team trainings
- Advise on eCRF design and automated data checks
- Review ICFs, lab alerts, and recruitment activities
- Contribute to regulatory and ethics committee responses
- Address medical questions from investigators
- Support adjudication and Data Monitoring Committee processes
- Provide state-of-the-art medical expertise to project teams
- Execute medical oversight during trial preparation and conduct
- Manage medical reporting for clinical trials
- Serve as a core member of the Trial Team
- Participate in the Evidence Network for the asset
Work Experience
- 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- ICH-GCP regulations
Benefits
Flexible Working
- Home office
- Flexible working hours
- Flexible working time models
More Vacation Days
- Additional bridge-days off
Free or Subsidized Food
- Subsidized staff restaurant
- Subsidized cafeteria
- Vegetarian and vegan options
Learning & Development
- Learning and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim 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
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
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