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Clinical Project Associate I in Jacksonville, FL at Integrated Resources, Inc

Date Posted: 11/8/2018

Job Snapshot

Job Description

Position Description
Job Title:
Clinical Project Associate I
Position Summary:
Documentation specialist to work with R&D project managers and Quality Engineers on preparation of GNPP design control documents as per QA VS-0030. Strong attention to detail and accuracy in transcription from original or draft documents is required. Adheres to environmental policy, procedures, and supports department environmental objectives.
Essential Functions/Responsibilities
Documentation support and process follow up including data entry and verification.
Act as liaison with internal and external department partners to facilitate effective system and documentation use and adherence to compliance.
Audits of outstanding approved documents to monitor document lifecycle status to ensure compliance
Provide routine sample management support and coordination of sample movement within TeamCenter systems
Reviewing, approving and making documents effective
Under general supervision, works within established guidelines and has flexibility as to method, priority and timing of job duties. Requires some amount of initiative and judgment.
Qualifications:
Minimum education required for competent performance: Bachelor's Degree in Science/technical field preferred
Minimum experience: 2 years of project management and/or documentation control related experience in a regulated environment.
Volume or unit measure of job duties: 10 to 15 technical documents reviewed and checked per project.
Equipment usage and abilities needed: MS Office suite of software. JJVC Teamcenter (JJVC will train)
Conditions & Physical Demands of Job: Office job that works closely with R&D, Quality Engineers and project teams.
Travel Required: NO