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Clinical Data/Document Coordinator Job
Eingestellt von Yoh
Gesuchte Skills: Support, Adobe
Projektbeschreibung
What You'll Be Doing:
- Overall position is considered document management support and data entry/review.
- Individual will be working with the site regulatory product management to update licensing commitment documents to support industrial operations.
- Individual will be required to update existing documentation into a new template aligning information with country specific licenses, route for review, track and incorporate comments and route for final approval.
- Individual will act as a liaison between Regulatory Affairs and Industrial Operations.
What You Need to Bring to the Table:
- Working knowledge of Adobe Acrobat and Word a must.
- Although not considered a technical writing position, these skills will be useful.
- Prior work in pharmaceutical regulatory affairs and/or pharmaceutical quality industry is a must Project management experience is desired Individual must be able to work independently
- Associate degree or higher with three to five (3-5) years of experience with data management.
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: CLINICAL
MONJOBJ2WMIDATL
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Pennsylvania, 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:
Medien/Design, Sonstiges