Vakante Jobangebote finden Sie unter Projekte.
Clinical Records Specialist Job
Eingestellt von Yoh
Gesuchte Skills: Client
Projektbeschreibung
WHAT YOU'LL BE DOING:
- Responsible for preparing: Filling and archiving of clinical trial documents including CRFs and all documents related to the Clinical Trial Master File (TMF) CRF and related clinical documents for submission CD roms for the investigator study file
- Strong collaboration with Record Coordinator and T.O staff.
- Works in close collaboration with Trial Operations teams to provide services for trial Record management, from study set-up to closure.
- These records include CRFs and all documents for the clinical trial master file.
- Perform daily tasks associated with initial receipt and quality control of clinical trial documents for filling and archiving.
- Involved in the preparation of the Clinical Study Report (CSR) appendices into the document repository system.
- Assist in the preparation and QC of documents for submission to regulatory agencies. Perform the data entry in archiving tools for the tracking of all documents
- Perform QC and all supportive activities on the preparation of CD rom for the Investigator Study File.
- Communicate effectively with study teams.
YOU NEED TO BRING TO THE TABLE:
- High School graduate
- The candidate should be proficient in Microsoft applications and technically savy to be able to learn different electronic repository systems
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: CLINICAL
MONJOBJ2WMIDATL
Ref:
SFSF: LS
Projektdetails
-
Einsatzort:
Bridgewater, Vereinigte Staaten
-
Projektbeginn:
asap
-
Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung