ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Full-timeWith HomeofficeExperienced
Mannheim
New Job?Nejo!
The AI Job Search Engine
ICICON plc
Study Start Up Associate(m/w/x)
Mannheim
Full-timeWith Home OfficeJunior
Nejo AI Summary
Preparing and submitting clinical trial and ethics committee applications in a global clinical research organization. Bachelor's degree in life sciences required; previous clinical research experience preferred. Coordination across diverse global clinical studies.
Requirements
- Bachelor's degree in life sciences or related field
- Previous experience in clinical research or regulatory affairs (preferred)
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal skills
- Ability to collaborate with cross-functional teams
- Ability to work independently
- Ability to manage multiple tasks simultaneously
- Ability to work in a fast-paced environment
Tasks
- Prepare and submit clinical trial applications.
- Prepare and submit ethics committee submissions.
- Coordinate with internal and external stakeholders.
- Obtain study approvals and authorizations.
- Maintain accurate regulatory submission and approval records.
- Support study teams developing protocols.
- Support study teams developing informed consent forms.
- Support study teams developing investigator brochures.
- Participate in study start-up meetings.
- Provide input on regulatory requirements and timelines.
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
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
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.
Not a perfect match?
- 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Senior Clinical Trial Manager(m/w/x)
Full-timeRemoteSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorMannheim
ICICON plc
Study Start Up Associate(m/w/x)
Mannheim
Full-timeWith Home OfficeJunior
Nejo AI Summary
Preparing and submitting clinical trial and ethics committee applications in a global clinical research organization. Bachelor's degree in life sciences required; previous clinical research experience preferred. Coordination across diverse global clinical studies.
Requirements
- Bachelor's degree in life sciences or related field
- Previous experience in clinical research or regulatory affairs (preferred)
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal skills
- Ability to collaborate with cross-functional teams
- Ability to work independently
- Ability to manage multiple tasks simultaneously
- Ability to work in a fast-paced environment
Tasks
- Prepare and submit clinical trial applications.
- Prepare and submit ethics committee submissions.
- Coordinate with internal and external stakeholders.
- Obtain study approvals and authorizations.
- Maintain accurate regulatory submission and approval records.
- Support study teams developing protocols.
- Support study teams developing informed consent forms.
- Support study teams developing investigator brochures.
- Participate in study start-up meetings.
- Provide input on regulatory requirements and timelines.
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance
- Health assessments
Retirement Plans
- Retirement planning
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
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.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Not a perfect match?
- ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Full-timeWith HomeofficeExperiencedMannheim - 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Senior Clinical Trial Manager(m/w/x)
Full-timeRemoteSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorMannheim - ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Full-timeWith HomeofficeSeniorMannheim