IQVIA
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeExperienced
Frankfurt am Main
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ICICON plc
Site Activation Lead(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Managing day-to-day clinical trial site activation and country distribution plans for a global CRO. Solid site start-up and activation experience required. 5+ years clinical research experience, Bachelor's degree preferred.
Requirements
- Solid site start-up and activation experience
- Ability to manage competing priorities
- Team development ability
- Bachelor's Degree, preferably in life sciences
- Minimum 5 years Clinical Research experience
- Focus on Start-Up experience
- Strong project management skills
- Deep understanding of regulatory processes
- Deep understanding of submission processes in various countries
- Excellent written communication abilities
- Excellent verbal communication abilities
- Proven ability to work efficiently to tight deadlines
- Proven ability to manage multiple priorities
- Willingness to travel as required (approximately 30%) across Germany
- Fluent in German
- Fluent in English
- Encouraged to apply regardless of meeting all requirements
Tasks
- Advance clinical trial start-up activities
- Understand client objectives
- Assist in developing country and site distribution plans
- Manage day-to-day site start-up and activation
- Ensure adherence to sponsor timelines and expectations
- Comply with ICON and client KPIs, SOPs, and regulatory standards
- Create comprehensive site activation plans
- Conduct studies according to activation plans
- Lead sponsor initiatives and meetings
- Facilitate bid defenses, project updates, and status calls
- Optimize performance and collaboration
- Ensure successful study outcomes
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Native
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible country-specific optional benefits
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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ICICON plc
Site Activation Lead(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Managing day-to-day clinical trial site activation and country distribution plans for a global CRO. Solid site start-up and activation experience required. 5+ years clinical research experience, Bachelor's degree preferred.
Requirements
- Solid site start-up and activation experience
- Ability to manage competing priorities
- Team development ability
- Bachelor's Degree, preferably in life sciences
- Minimum 5 years Clinical Research experience
- Focus on Start-Up experience
- Strong project management skills
- Deep understanding of regulatory processes
- Deep understanding of submission processes in various countries
- Excellent written communication abilities
- Excellent verbal communication abilities
- Proven ability to work efficiently to tight deadlines
- Proven ability to manage multiple priorities
- Willingness to travel as required (approximately 30%) across Germany
- Fluent in German
- Fluent in English
- Encouraged to apply regardless of meeting all requirements
Tasks
- Advance clinical trial start-up activities
- Understand client objectives
- Assist in developing country and site distribution plans
- Manage day-to-day site start-up and activation
- Ensure adherence to sponsor timelines and expectations
- Comply with ICON and client KPIs, SOPs, and regulatory standards
- Create comprehensive site activation plans
- Conduct studies according to activation plans
- Lead sponsor initiatives and meetings
- Facilitate bid defenses, project updates, and status calls
- Optimize performance and collaboration
- Ensure successful study outcomes
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Native
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Flexible country-specific optional benefits
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- IQVIA
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