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Principal CRA
Eingestellt von Aerotek
Projektbeschreibung
This person be responsible for duties including:
- Supervising and coordinating all aspects of the clinical studies
- Conducting co-monitoring as required
- Drafting and coordinating review of relevant documents such as protocols, informed consents, case report forms, monitoring plans, etc.
- Contributing to the development of study budgets
- Maintaining study timelines
- Contributing to the development of RFPs and participating in the selection of CROs/vendors as well as managing them
- Coordinating review of data listings and preparing clinical study reports
Qualifications include:
- A minimum of 4 years of experience performing related duties
- Experience in study management/coordination of multinational clinical trials
- UK Pharmaceutical experience
- Monitoring experience
- In depth knowledge of FDA and EMEA regulations, ICH guidelines, and GCPs
Interested candidates can feel free to send CVs directly or contact Andrew directly.
Allegis Group Limited and Aston Carter Limited operate Employment Businesses and Agencies and are companies within the Allegis Group Inc. group of companies, the fourth largest staffing company in the world, (collectively referred to as the "Allegis Group"). TEKsystems and Aerotek are divisions of Allegis Group Limited. Applicant data will be treated in accordance with the Allegis Group's Privacy Notice.
Projektdetails
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Einsatzort:
Middlesex, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
12 months
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges