Aktualne oferty pracy związane z Clinical Research Associate - Warszawa, Mazovia - Allergan
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Senior Clinical Research Professional
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Clinical Research Associate
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Clinical Research Operations Associate
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Clinical Research Associate
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Clinical Research Associate Lead
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Clinical Research Associate
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Senior Clinical Research Manager
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Clinical Research Associate II
4 dni temu
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Experienced Clinical Research Associate SM
5 dni temu
Warszawa, Mazovia, Polska TN Poland Pełny etatSocial network you want to login/join with:Experienced Clinical Research Associate SM, WarsawClient:IQVIALocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:23dbfc09693dJob Views:2Posted:17.03.2025Expiry Date:01.05.2025Job Description:Our team is growing, join us on our mission to drive healthcare forwardWhat We Offer / USPsThe...
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Clinical Research Associate
3 dni temu
Warszawa, Mazovia, Polska IQVIA Argentina Pełny etatIQVIA Biotech is hiring Clinical Research AssociatesJoin IQVIA today and make an impact on patients' outcomeJob OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor...
Clinical Research Associate
2 tygodni temu
We are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the conduct of clinical trials.
The primary responsibilities of this position include:
- Supporting the organization, management, and execution of projects;
- Ensuring compliance with Good Clinical Practices (GCPs), ICH Guidelines, and local regulations;
- Managing clinical investigative sites across multiple protocols and therapeutic areas;
- Ensuring the integrity and quality of data submitted from study sites;
- Conducting independent visits and monitoring activities;
- Training study site personnel on protocol and regulatory requirements;
- Facilitating Quality Assurance Audit processes and ensuring regulatory inspection readiness;
- Preparing and submitting written reports on monitoring and administrative activities;
This is an exciting opportunity for someone looking to advance their career in clinical research. If you have a strong understanding of GCPs, ICH Guidelines, and local regulations, and experience in conducting clinical research, we encourage you to apply.
