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Study Start Up Associate I(m/w/x)
Description
As a Study Start Up Associate I, you will facilitate the initiation of clinical trials by preparing regulatory documents, coordinating approvals, and supporting study teams in developing essential materials. This role is crucial in advancing innovative treatments.
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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
Education
Work Experience
approx. 1 - 4 years
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
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
- 176 ICON Clinical Research Germany GmbHFull-timeRemoteExperiencedFrankfurt am Main
- ICON plc
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Clinical Research Associate (CRA)(m/w/x)
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Study Start Up Associate I(m/w/x)
The AI Job Search Engine
Description
As a Study Start Up Associate I, you will facilitate the initiation of clinical trials by preparing regulatory documents, coordinating approvals, and supporting study teams in developing essential materials. This role is crucial in advancing innovative treatments.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
approx. 1 - 4 years
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
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
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
- 176 ICON Clinical Research Germany GmbH
Study Start Up Associate II(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate II(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 plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - ICON plc
CRA I (sponsor dedicated)(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main