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Clinical Study Coordinator Job
Eingestellt von Yoh
Gesuchte Skills: Client
Projektbeschreibung
What You'll Be Doing:
- The primary work involved is to sort through boxes of paper records to identify which documents must be maintained as per GCP requirements and the Global Records Retention Schedule.
- Records retention for long term archival includes both paper and electronic format, so work involves scanning and converting documents to electronic format and then posting to the correct TMF archival location.
What You Need to Bring to the Table:
- BA/BS in life science or related field
- Candidates must have knowledge/experience/familiarity with GCP required clinical research documents, construction and maintenance of Trial Master File (structure and content), and records management in pharmaceutical or CRO industry.
- Skills in use of or familiarity with a computer, document scanner, copy machine required.
- Ability to work with moderate independence after completion of training is required.
- Past experience working at a pharmaceutical company or CRO in the creation, maintenance, and auditing of GCP records highly beneficial and preferred.
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a DayJ2W: CLINICAL
MONJOBJ2WSEMW
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Durham, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung