BioNTech SE
Senior Director, Safety Sciences Lead(m/w/x)
Full-timeOn-siteSenior
Mainz, München
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BOBoehringer Ingelheim
Senior Triage and Review Specialist(m/w/x)
Ingelheim am Rhein
Full-timeOn-siteSenior
Nejo AI Summary
Processing adverse event data for investigational and marketed drugs. Bachelor's degree and long-standing pharmacovigilance experience required. Independent decision-making and workload prioritization skills.
Requirements
- Bachelor's degree in health care/life science or medical information/data science
- Long-standing pharmaceutical industry experience, specifically Pharmacovigilance
- Independent decision-making and problem-solving skills
- Workload prioritization and stress management skills
- Strong communication and interpersonal skills
- Proficiency in collecting, interpreting, and reconciling medical information in English
- Fluent English skills, written and spoken
Tasks
- Guide vendors and colleagues on adverse event intake and processing
- Complete individual case safety reports within strict timelines
- Review Phase II and III clinical trial protocols for PV regulatory aspects
- Identify and request missing medical data for adverse event cases
- Act as a GCM representative in project teams and working groups
- Collaborate with GPV risk management physicians
- Contribute to global safety platform projects
- Coordinate phase II and III clinical trials
- Provide guidance on standard medical inquiries
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
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
Senior Triage and Review Specialist(m/w/x)
Ingelheim am Rhein
Full-timeOn-siteSenior
Nejo AI Summary
Processing adverse event data for investigational and marketed drugs. Bachelor's degree and long-standing pharmacovigilance experience required. Independent decision-making and workload prioritization skills.
Requirements
- Bachelor's degree in health care/life science or medical information/data science
- Long-standing pharmaceutical industry experience, specifically Pharmacovigilance
- Independent decision-making and problem-solving skills
- Workload prioritization and stress management skills
- Strong communication and interpersonal skills
- Proficiency in collecting, interpreting, and reconciling medical information in English
- Fluent English skills, written and spoken
Tasks
- Guide vendors and colleagues on adverse event intake and processing
- Complete individual case safety reports within strict timelines
- Review Phase II and III clinical trial protocols for PV regulatory aspects
- Identify and request missing medical data for adverse event cases
- Act as a GCM representative in project teams and working groups
- Collaborate with GPV risk management physicians
- Contribute to global safety platform projects
- Coordinate phase II and III clinical trials
- Provide guidance on standard medical inquiries
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
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.
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