Document Control Specialist jobs in Piscataway, NJ

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CLINICAL DOCUMENT SPECIALIST - FULL TIME DAY

Responsibilities:Bridging the gap between the Physician documentation and the Coding professional through compliance review of inpatient charts. Provide educational materials and seminars to physicians, coding staff, and other int...

CompanyRwjbarnabas Health
AddressNew Brunswick, NJ
CategoryInformation Technology
Job typeFull-Time
Date Posted 2 months ago See detail

Clinical Document Specialist - Full Time Day

Rwjbarnabas Health

New Brunswick, NJ

Responsibilities:Bridging the gap between the Physician documentation and the Coding professional through compliance review of inpatient charts. Provide educational materials and seminars to physicians, coding staff, and other int...

Inventory Control Specialist

Johnson & Johnson

Raritan, NJ

Performs Inventory Control activities maintaining accurate records of incoming and outgoing products and supplies. Through digital and manual counting you will identify discrepancies with inventory reports and provide these repor...

Inventory Control Specialist - GWW - US

Sysco

Sayreville, NJ

Reconcile PeopleSoft and High Jump balances on a daily basis by utilizing various reports (i.e., Inventory Reconciliation Report). Investigate and resolve BCT Errors by analyzing transaction flow in both systems, understanding the...

Inventory Control Specialist

Johnson & Johnson

Somerset, NJ

$50,000 - $80,500 a year

Partner with management and engineering in the creation and implementation of new processes. Align all Inventory Control (including refusals, recalls, etc.) documents to all WMS requirements (print screens, terminology, process fl...

Clinical Document Specialist (RN) - Full-Time Day

Rwjbarnabas Health

Somerville, NJ

Responsibilities:Bridging the gap between the Physician documentation and the Coding professional through compliance review of inpatient charts. Provide educational materials and seminars to physicians, coding staff, and other int...

Senior Specialist, Non-clinical Pharmacology Document Writing (Hybrid)

Merck

Rahway, NJ

Primary responsibility is writing and preparing nonclinical pharmacology regulatory document submission sections and study reports to support the development of therapeutic agents and vaccines.. This includes but is not limited to...