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Clinical Trial Manager(m/w/x)
Description
End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
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Requirements
- •Degree in medicine, science, or equivalent
- •Ability to drive clinical study deliverables
- •Expertise in designated therapeutic area
- •Prior monitoring experience preferred
- •Ability to travel up to 20%
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Plan and manage all clinical trial aspects
- •Ensure adherence to timelines and budgets
- •Maintain high quality standards
- •Collaborate with cross-functional teams
- •Establish and implement trial protocols
- •Build relationships with investigators and stakeholders
- •Ensure compliance with international and local regulations
- •Adhere to ethical guidelines
- •Make critical decisions on trial design
- •Manage vendor selection and risk assessment
Languages
English – Business Fluent
Benefits
Healthcare & Fitness
- •Health insurance offerings
- •Health assessments
Retirement Plans
- •Retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
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Clinical Trial Manager(m/w/x)
The AI Job Search Engine
Description
End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in medicine, science, or equivalent
- •Ability to drive clinical study deliverables
- •Expertise in designated therapeutic area
- •Prior monitoring experience preferred
- •Ability to travel up to 20%
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Plan and manage all clinical trial aspects
- •Ensure adherence to timelines and budgets
- •Maintain high quality standards
- •Collaborate with cross-functional teams
- •Establish and implement trial protocols
- •Build relationships with investigators and stakeholders
- •Ensure compliance with international and local regulations
- •Adhere to ethical guidelines
- •Make critical decisions on trial design
- •Manage vendor selection and risk assessment
Languages
English – Business Fluent
Benefits
Healthcare & Fitness
- •Health insurance offerings
- •Health assessments
Retirement Plans
- •Retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Childcare
- •Childcare vouchers
Company Bike
- •Bike purchase schemes
Corporate Discounts
- •Discounted gym memberships
Public Transport Subsidies
- •Subsidised travel passes
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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