ICON plc
Study Start Up Associate I(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main
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17176 ICON Clinical Research Germany GmbH
Study Start Up Associate II(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Leading regulatory document preparation for clinical trials, coordinating approvals with stakeholders. 2+ years in clinical research or regulatory affairs, with strong regulatory understanding, required. Global clinical research setting; innovative treatments focus.
Requirements
- Bachelor's degree in life sciences or related field
- Minimum of 2 years of experience in clinical research or regulatory affairs
- Strong understanding of regulatory requirements and guidelines for clinical trials
- Excellent organizational and project management skills
- Excellent communication and interpersonal skills
Tasks
- Lead preparation and submission of regulatory documents
- Coordinate with internal and external stakeholders for approvals
- Manage records of regulatory submissions and correspondence
- Provide guidance on regulatory requirements to study teams
- Participate in process improvement initiatives for study start-up
Work Experience
- 2 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 176 ICON Clinical Research Germany GmbH 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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17176 ICON Clinical Research Germany GmbH
Study Start Up Associate II(m/w/x)
Frankfurt am Main
Full-timeRemoteExperienced
Nejo AI Summary
Leading regulatory document preparation for clinical trials, coordinating approvals with stakeholders. 2+ years in clinical research or regulatory affairs, with strong regulatory understanding, required. Global clinical research setting; innovative treatments focus.
Requirements
- Bachelor's degree in life sciences or related field
- Minimum of 2 years of experience in clinical research or regulatory affairs
- Strong understanding of regulatory requirements and guidelines for clinical trials
- Excellent organizational and project management skills
- Excellent communication and interpersonal skills
Tasks
- Lead preparation and submission of regulatory documents
- Coordinate with internal and external stakeholders for approvals
- Manage records of regulatory submissions and correspondence
- Provide guidance on regulatory requirements to study teams
- Participate in process improvement initiatives for study start-up
Work Experience
- 2 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 176 ICON Clinical Research Germany GmbH 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
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.
Not a perfect match?
- ICON plc
Study Start Up Associate I(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Study Start Up Specialist(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Clinical Research Associate II - FSP(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON Clinical Research Germany GmbH
CRA II Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Lead Assistant(m/w/x)
Full-timeRemoteSeniorFrankfurt am Main