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Study Start Up Associate(m/w/x)
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.
Anforderungen
- 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
Aufgaben
- 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.
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Noch nicht perfekt?
- ICON Clinical Research Germany GmbHVollzeitmit HomeofficeBerufserfahrenMannheim
- 176 ICON Clinical Research Germany GmbH
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Study Start Up Associate(m/w/x)
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.
Anforderungen
- 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
Aufgaben
- 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.
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Über das Unternehmen
ICON plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Noch nicht perfekt?
- ICON Clinical Research Germany GmbH
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