Clinical Documentation Specialist Job

DOCUMENTATION COORDINATOR needed for a CONTRACT opportunity with Yoh's client located in WOODCLIFF LAKE, NJ.

The Big Picture - Top Skills You Should Possess:
- Perform daily document management activities such as Review, Processing, Filing of Clinical Trial Master File documents.
- Quality Control review of Regulatory Documents.
- Coordinate with eTMF vendor for TMF set-up and processing of TMF documents.
- Development of user manuals.
- Scanning and storage of Clinical Operation documentation such as CRFs and Trial Master files.
- Must have strong document management skills, including experience with review of Regulatory Documents, be detail oriented, organized, quality driven and able to work in a team environment under tight deadlines.
- Excellent written, verbal, and interpersonal communication skills.

What You Need to Bring to the Table:
- Bachelor's Degree preferred.
- Working knowledge of Microsoft Word, Microsoft Excel, Adobe Acrobat, and electronic document management systems, preferably Documentum.
- Agility with ClinOps databases preferred.
- Basic knowledge of CFR, GCP & ICH Guidelines.
- Two (2) plus years Pharma experience

OPPORTUNITY IS CALLING, APPLY NOW!

RECRUITER: Krista Leach

Yoh, a DayJ2W: PROF

MONJOBJ2WPACNW

Ref:

SFSF: LS