Aktuelle Jobs im Zusammenhang mit Clinical Research Associate Ii - Hamburg - Alimentiv
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Clinical Research Associate
vor 1 Woche
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Clinical Research Associate
vor 2 Wochen
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Freelance Clinical Research Associate
vor 1 Woche
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Freelance Clinical Research Associate
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Research Associate
vor 2 Wochen
Hamburg, Deutschland Universität Hamburg VollzeitResearch Associate - 28 Subsection 1 HmbHG (2 positions) - InstitutionFaculty of Psychology and Human Movement Science, Department Cognitive Psychology Salary levelEGR. 13 TV-L Start date01.04.2025, the initial fixed term is three years. Application deadline06.01.2025 Scope of workpart-time Weekly hours75 % of standard work hours per...
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Research Associate
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Clinical Research Associate
vor 2 Wochen
Hamburg, Deutschland AstraZeneca VollzeitInnovativ, dynamisch und nachhaltig: Als eines der weltweit führenden Unternehmen der forschenden Arzneimittelindustrie bieten wir bei AstraZeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Denn für uns steht fest: Forschung bildet das Fundament unserer aller Zukunft. Wir bei AstraZeneca stellen die Wissenschaft in den...
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Research Associate
Vor 3 Tagen
Hamburg, Deutschland Universität Hamburg VollzeitResearch Associate - 28 Subsection 3 HmbHG - InstitutionFaculty of Mathematics, Informatics and Natural Sciences, Department of Physics, Institute for Nanostructure and Solid State Physics Salary levelEGR. 13 TV-L Start date01.04.2025, permanent Application deadline20.12.2024 Scope of workfull-time position suitable for...
Clinical Research Associate Ii
vor 2 Wochen
This is an exciting opportunity to join a niche GI CRO and recognized expert in IBD and Clinical Trial Design. Alimentiv is a culturally diverse organization that is committed to transforming human health.
As a Clinical Research Associate II, you will Performs and coordinates all aspects of the clinical site monitoring services, assessing for protocol and regulatory compliance. Responsibilities include driving investigative site and patient recruitment, conducting source data verification, assessing drug accountability, data collection, (regulatory) document collection, performing qualification, initiation, monitoring and close out visits at investigational sites in accordance with corporate, sponsor and regulatory (ICH GCP and other) standards and guidelines
**What you bring**
- A college diploma/degree and 1-3 years of related experience.
- Self-motivated
- Strong communication skills
- Commitment to achieving positive results.
- Strong attention to detail
- Collaborative & team player
- Desire to engage in continuous learning and self-development.
**Rewards**
- Positive, healthy, and peaceful work environment
- Meaningful work
- Different employee experience: competitive and innovative
- Less travel
- Commitment to training & development
- Comprehensive Total Rewards Package
- Career progression
**WORKING CONDITIONS**:
Home-based
Regular travel
- Accommodations for job applicants with disabilities are available upon request.
LI-Remote
