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Medical Monitor (Gastroenterology)(m/w/x)
Description
In this role, you will be the key medical contact for clinical trials, ensuring participant safety and compliance with regulations. Your daily responsibilities will include advising teams, reviewing clinical data, and collaborating on development plans.
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
- •Gastroenterology Fellowship certification
- •Minimum of 10 years of experience as a practicing MD
- •Prior research and/or industry experience
- •Full working proficiency in English
- •Proficiency with MS Office applications
- •Communication, presentation, and analytical skills
- •Teamwork, problem-solving, and detail-oriented skills
Education
Work Experience
10 years
Tasks
- •Serve as the medical point of contact for project teams, study sites, and sponsors
- •Advise clients and teams on medical matters related to clinical trials
- •Collaborate on clinical development plans and protocols
- •Review investigator brochures and annual reports
- •Analyze clinical data to ensure participant safety
- •Verify the accuracy and completeness of reported trial data
- •Address safety issues raised by sites and the study team
- •Support medical data review processes
- •Participate in bid defense meetings and proposal activities
- •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 (Gastroenterology)(m/w/x)
The AI Job Search Engine
Description
In this role, you will be the key medical contact for clinical trials, ensuring participant safety and compliance with regulations. Your daily responsibilities will include advising teams, reviewing clinical data, and collaborating on development plans.
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
- •Gastroenterology Fellowship certification
- •Minimum of 10 years of experience as a practicing MD
- •Prior research and/or industry experience
- •Full working proficiency in English
- •Proficiency with MS Office applications
- •Communication, presentation, and analytical skills
- •Teamwork, problem-solving, and detail-oriented skills
Education
Work Experience
10 years
Tasks
- •Serve as the medical point of contact for project teams, study sites, and sponsors
- •Advise clients and teams on medical matters related to clinical trials
- •Collaborate on clinical development plans and protocols
- •Review investigator brochures and annual reports
- •Analyze clinical data to ensure participant safety
- •Verify the accuracy and completeness of reported trial data
- •Address safety issues raised by sites and the study team
- •Support medical data review processes
- •Participate in bid defense meetings and proposal activities
- •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.
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