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Senior Clinical Trial Manager(m/w/x)
Description
As a Senior Clinical Trial Manager, you will be at the forefront of clinical study delivery, managing budgets, training teams, and ensuring smooth enrollment processes. This role involves collaborating with various stakeholders and addressing risks to enhance clinical outcomes.
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Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •4 year degree or equivalent combination of education & experience
- •Demonstrated ability to drive clinical deliverables of a study
- •Subject matter expertise in designated therapeutic area
- •Prior monitoring experience preferred
- •Ability to travel up to 20%
- •Fluency in local language - both written & verbal
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Oversee the clinical budget
- •Develop monitoring plans and tools
- •Train Clinical Research Associates (CRAs)
- •Drive enrollment and study start-up activities
- •Review trip reports
- •Implement corrective and preventative action plans
- •Liaise with the Sponsor, vendors, and cross-functional teams
- •Identify and mitigate risks impacting clinical delivery
- •Provide reporting and metrics on clinical activities
- •Participate in Sponsor, Investigator, and bid defense meetings
Languages
local – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Competitive retirement planning
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Additional Allowances
- •Flexible optional benefits
- ICON plcFull-time/Part-timeRemoteSeniorFrankfurt am Main
- GBG Forschungs GmbH
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Senior Clinical Trial Manager(m/w/x)
The AI Job Search Engine
Description
As a Senior Clinical Trial Manager, you will be at the forefront of clinical study delivery, managing budgets, training teams, and ensuring smooth enrollment processes. This role involves collaborating with various stakeholders and addressing risks to enhance clinical outcomes.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •4 year degree or equivalent combination of education & experience
- •Demonstrated ability to drive clinical deliverables of a study
- •Subject matter expertise in designated therapeutic area
- •Prior monitoring experience preferred
- •Ability to travel up to 20%
- •Fluency in local language - both written & verbal
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Oversee the clinical budget
- •Develop monitoring plans and tools
- •Train Clinical Research Associates (CRAs)
- •Drive enrollment and study start-up activities
- •Review trip reports
- •Implement corrective and preventative action plans
- •Liaise with the Sponsor, vendors, and cross-functional teams
- •Identify and mitigate risks impacting clinical delivery
- •Provide reporting and metrics on clinical activities
- •Participate in Sponsor, Investigator, and bid defense meetings
Languages
local – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Competitive retirement planning
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Additional Allowances
- •Flexible optional benefits
About the Company
176 ICON Clinical Research Germany GmbH
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovative treatments.
- ICON plc
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