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Study Site Management Specialist(m/w/x)
Leading clinical trial start-up and site activation delivery for healthcare intelligence projects at a global clinical research organization. 5 years clinical research experience and a life sciences Bachelor's Degree required. Various annual leave entitlements, global employee assistance program.
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
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
Work Experience
- 5 years
Education
- Bachelor's degree
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
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Study Site Management Specialist(m/w/x)
Leading clinical trial start-up and site activation delivery for healthcare intelligence projects at a global clinical research organization. 5 years clinical research experience and a life sciences Bachelor's Degree required. Various annual leave entitlements, global employee assistance program.
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
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
Work Experience
- 5 years
Education
- Bachelor's degree
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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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