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Study Site Management Specialist(m/w/x)
Description
As a Site Activation Lead, you will drive the start-up of clinical trials by aligning with client goals and managing site activation plans. Your role involves overseeing project delivery, ensuring compliance, and leading key communications to achieve successful outcomes.
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Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor’s Degree in life sciences
- •Minimum of 5 years of experience in Clinical Research
- •Strong project management skills
- •Excellent written and verbal communication abilities
- •Proven ability to work efficiently to tight deadlines
Education
Work Experience
5 years
Tasks
- •Lead clinical trial start-up activities
- •Understand client objectives and develop site distribution plans
- •Oversee daily site activation delivery for assigned projects
- •Ensure compliance with sponsor timelines and ICON/client KPIs
- •Create comprehensive site activation plans for each project
- •Conduct kick-off meetings and project updates
- •Facilitate bid defenses and status calls
- •Utilize project management skills to enhance collaboration
Languages
English – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Retirement planning offerings
Mental Health Support
- •Global Employee Assistance Programme
Other Benefits
- •Life assurance
Additional Allowances
- •Flexible optional benefits
- 176 ICON Clinical Research Germany GmbHFull-timeWith HomeofficeSeniorMannheim
- Penumbra
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Study Site Management Specialist(m/w/x)
The AI Job Search Engine
Description
As a Site Activation Lead, you will drive the start-up of clinical trials by aligning with client goals and managing site activation plans. Your role involves overseeing project delivery, ensuring compliance, and leading key communications to achieve successful outcomes.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor’s Degree in life sciences
- •Minimum of 5 years of experience in Clinical Research
- •Strong project management skills
- •Excellent written and verbal communication abilities
- •Proven ability to work efficiently to tight deadlines
Education
Work Experience
5 years
Tasks
- •Lead clinical trial start-up activities
- •Understand client objectives and develop site distribution plans
- •Oversee daily site activation delivery for assigned projects
- •Ensure compliance with sponsor timelines and ICON/client KPIs
- •Create comprehensive site activation plans for each project
- •Conduct kick-off meetings and project updates
- •Facilitate bid defenses and status calls
- •Utilize project management skills to enhance collaboration
Languages
English – Business Fluent
Benefits
More Vacation Days
- •Various annual leave entitlements
Healthcare & Fitness
- •Health insurance offerings
Retirement Plans
- •Retirement planning offerings
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.
- 176 ICON Clinical Research Germany GmbH
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