3121 MSD Gesellschaft m.b.H.
Medical Advisor Vaccines(m/w/x)
Full-timeWith HomeofficeExperienced
Wien
from 67,600 / year
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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 for clinical trials, developing quality monitoring plans and reviewing data. MD with 4+ years active clinical practice required. Home office, flexible hours, additional days off.
Requirements
- Medical degree (MD) with clinical training
- At least 4 years active clinical practice
- Specialization in Internal Medicine or General Practice (advantage)
- Professional experience in pharmaceutical industry or CRO (ideally medical/project roles)
- Solid understanding of ICH-GCP regulations
- Solid understanding of clinical research processes
- Solid understanding of relevant regulatory guidance
- Strong analytical skills
- Strong communication skills
- Structured working style
- Ability to collaborate in international environment
- Proficiency in medical data review/analysis
- Fluency in English (written and spoken)
Tasks
- Provide medical oversight and support throughout clinical trials
- Collaborate with cross-functional teams to ensure high-quality medical content
- Develop and maintain the Clinical Quality Monitoring Plan
- Conduct ongoing medical data review and support risk-based quality management
- Define key protocol deviations and ensure compliance
- Train investigators and study teams on medical aspects
- Design eCRF, automated data checks, ICF, and lab alerts
- Contribute to feasibility and recruitment activities
- Respond to regulatory and ethics committee inquiries
- Act as primary contact for medical questions from investigators
- Participate in adjudication and Data Monitoring Committee processes
Work Experience
- 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
Learning & Development
- Diverse training 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 for clinical trials, developing quality monitoring plans and reviewing data. MD with 4+ years active clinical practice required. Home office, flexible hours, additional days off.
Requirements
- Medical degree (MD) with clinical training
- At least 4 years active clinical practice
- Specialization in Internal Medicine or General Practice (advantage)
- Professional experience in pharmaceutical industry or CRO (ideally medical/project roles)
- Solid understanding of ICH-GCP regulations
- Solid understanding of clinical research processes
- Solid understanding of relevant regulatory guidance
- Strong analytical skills
- Strong communication skills
- Structured working style
- Ability to collaborate in international environment
- Proficiency in medical data review/analysis
- Fluency in English (written and spoken)
Tasks
- Provide medical oversight and support throughout clinical trials
- Collaborate with cross-functional teams to ensure high-quality medical content
- Develop and maintain the Clinical Quality Monitoring Plan
- Conduct ongoing medical data review and support risk-based quality management
- Define key protocol deviations and ensure compliance
- Train investigators and study teams on medical aspects
- Design eCRF, automated data checks, ICF, and lab alerts
- Contribute to feasibility and recruitment activities
- Respond to regulatory and ethics committee inquiries
- Act as primary contact for medical questions from investigators
- Participate in adjudication and Data Monitoring Committee processes
Work Experience
- 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
Learning & Development
- Diverse training 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
Not a perfect match?
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