176 ICON Clinical Research Germany GmbH
Study Start Up Associate II(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main
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ICICON plc
Study Start Up Associate I(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Preparing and submitting regulatory documents for clinical trial applications in a clinical research setting. Previous experience in clinical research or regulatory affairs required. Global employee assistance program available.
Requirements
- Bachelor's degree in life sciences or related field
- Previous experience in clinical research or regulatory affairs
- Strong attention to detail
- Organizational skills
- Excellent communication skills
- Interpersonal skills
- Ability to collaborate effectively with cross-functional teams
- Ability to work independently
- Ability to manage multiple tasks simultaneously
- Ability to work in a fast-paced environment
Tasks
- Assist in preparing regulatory documents
- Submit clinical trial applications
- Coordinate with stakeholders for approvals
- Maintain records of regulatory submissions
- Support development of study documents
- Participate in study start-up meetings
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
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
Study Start Up Associate I(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Preparing and submitting regulatory documents for clinical trial applications in a clinical research setting. Previous experience in clinical research or regulatory affairs required. Global employee assistance program available.
Requirements
- Bachelor's degree in life sciences or related field
- Previous experience in clinical research or regulatory affairs
- Strong attention to detail
- Organizational skills
- Excellent communication skills
- Interpersonal skills
- Ability to collaborate effectively with cross-functional teams
- Ability to work independently
- Ability to manage multiple tasks simultaneously
- Ability to work in a fast-paced environment
Tasks
- Assist in preparing regulatory documents
- Submit clinical trial applications
- Coordinate with stakeholders for approvals
- Maintain records of regulatory submissions
- Support development of study documents
- Participate in study start-up meetings
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
Retirement Plans
- Competitive retirement planning
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
- Flexible optional benefits
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?
- 176 ICON Clinical Research Germany GmbH
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Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
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