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Medical Monitor (Infectious Diseases)(m/w/x)
Description
In this role, you will provide essential medical insights for global clinical studies, ensuring participant safety while collaborating with various teams. Your daily responsibilities will include reviewing data, advising on protocols, and leading safety monitoring efforts.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical Doctor degree
- •Infectious Diseases Fellowship certification
- •Minimum of 10 years of experience as a practicing MD
- •Full working proficiency in English
- •Proficiency with MS Office applications
- •Communication, presentation and analytical skills
- •Problem-solving, teamwork and detail-oriented
Education
Work Experience
10 years
Tasks
- •Advise clients and project teams on medical matters
- •Collaborate on clinical development plans and protocols
- •Review clinical data to ensure participant safety
- •Verify accuracy and completeness of reported data
- •Address safety issues from sites and study teams
- •Support medical data review processes
- •Participate in bid defense meetings and proposals
- •Assist with pharmacovigilance activities
- •Identify trial risks and implement mitigation strategies
- •Organize and lead clinical development advisory boards
- •Ensure compliance with FDA, EMEA, ICH, and GCP guidelines
Tools & Technologies
Languages
English – Business Fluent
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Medical Monitor (Infectious Diseases)(m/w/x)
The AI Job Search Engine
Description
In this role, you will provide essential medical insights for global clinical studies, ensuring participant safety while collaborating with various teams. Your daily responsibilities will include reviewing data, advising on protocols, and leading safety monitoring efforts.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical Doctor degree
- •Infectious Diseases Fellowship certification
- •Minimum of 10 years of experience as a practicing MD
- •Full working proficiency in English
- •Proficiency with MS Office applications
- •Communication, presentation and analytical skills
- •Problem-solving, teamwork and detail-oriented
Education
Work Experience
10 years
Tasks
- •Advise clients and project teams on medical matters
- •Collaborate on clinical development plans and protocols
- •Review clinical data to ensure participant safety
- •Verify accuracy and completeness of reported data
- •Address safety issues from sites and study teams
- •Support medical data review processes
- •Participate in bid defense meetings and proposals
- •Assist with pharmacovigilance activities
- •Identify trial risks and implement mitigation strategies
- •Organize and lead clinical development advisory boards
- •Ensure compliance with FDA, EMEA, ICH, and GCP guidelines
Tools & Technologies
Languages
English – Business Fluent
About the Company
PSI CRO
Industry
Pharmaceuticals
Description
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
- BioNTech SE
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Full-timeOn-siteSeniorMainz, München