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Clinical Research Associate
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Ip
Projektbeschreibung
* Work closely with the Clinical Trial Managers, Medical Monitor, Drug Safety, Clinical Data Management, Regulatory/QA
* Contribute to preparation, review, and management of clinical protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research related documents
* Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations and study-specific manuals and procedures
* Responsible for review and IP release packages
* Participate in study close-down activities, e.g., reconciliation of un-used study supplies and clinical study report development
Desired Qualities:
* Cardiovascular, hematology and/or oncology (Phase I - 3) study experience
* Previous experience working with an electronic data capture system required
* Availability for potential travel domestically and internationally
Requirements:
* Minimum of 3-4 years relevant work experience of which ~ 1.5 years of site monitoring experience
* Experience in the pharmaceutical industry and working knowledge of GCP/ICH guidelines and the clinical development process
* BS/RN degree or equivalent
To find out more about Real please visit www.realstaffing.com
Projektdetails
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Einsatzort:
San Jose, California, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung