Die KI-Suchmaschine für Jobs
Study Start Up Associate I(m/w/x)
Beschreibung
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.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •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
Sprachen
Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- •Various annual leave entitlements
Gesundheits- & Fitnessangebote
- •Health insurance offerings
Betriebliche Altersvorsorge
- •Competitive retirement planning
Mentale Gesundheitsförderung
- •Global Employee Assistance Programme
Sonstige Vorteile
- •Life assurance
- •Flexible optional benefits
- 176 ICON Clinical Research Germany GmbHVollzeitRemoteBerufserfahrenFrankfurt am Main
- ICON plc
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Clinical Research Associate II(m/w/x)
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Clinical Research Associate II - FSP(m/w/x)
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Clinical Trial Assistant(m/w/x)
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Study Start Up Associate I(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
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.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •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
Sprachen
Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- •Various annual leave entitlements
Gesundheits- & Fitnessangebote
- •Health insurance offerings
Betriebliche Altersvorsorge
- •Competitive retirement planning
Mentale Gesundheitsförderung
- •Global Employee Assistance Programme
Sonstige Vorteile
- •Life assurance
- •Flexible optional benefits
Über das Unternehmen
ICON plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
- 176 ICON Clinical Research Germany GmbH
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Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
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