Scientific Resource Associate
Company: Planet Pharma
Posted on: May 12, 2022
This position has multi-functional responsibilities to provide
Scientific Coordination support in document administration, slide
scoring administration, and historical control database
ESSENTIAL DUTIES AND RESPONSIBILITIES:
--- Act as support for Scientific Coordination team.
--- Assist in the preparation, verification, print-editing, and
proofreading of regulated documents.
--- Assure that site document management strategies and regulatory
requirements for electronic documents are upheld.
--- Maintain the Genetic and In Vitro Toxicology historical
database files, with assistance.
--- Provide support for slide scoring via shipping, receiving,
archiving, coding/de-coding, etc., as needed.
--- Facilitate the signature/approval process for finalization of
protocols, amendments, and other regulated documents, as
--- Assist with protocol, procedure, or report template
maintenance, as appropriate.
--- Assist with scheduling of reports with Report Coordination
and/or QA in conjunction with SD/PIs and Scientific
--- Perform basic administrative tasks such as data entry, routine
narrative documents, photocopying and filing.
--- Perform all other related duties as assigned.
--- Education: Bachelor's degree (B.A./B.S.) or equivalent in
science or related discipline.
--- Experience: 0-2 years related experience in a laboratory or
scientific research environment.
--- An equivalent combination of education and experience may be
accepted as a satisfactory substitute for the specific education
and experience listed above.
--- Certification/Licensure: None
--- Other: Comprehensive knowledge of GLP and other federal
regulations and guidelines pertaining to preclinical research.
Proficient in word processing and spreadsheet software. Working
knowledge of computer operating systems and electronic
Keywords: Planet Pharma, Skokie , Scientific Resource Associate, Other , Skokie, Illinois
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