Report Writer

Alliance Pharma Inc.
Malvern, PA, United States
about 1 month ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Job source

Tech stack

Data Systems Laboratory Information Management Systems Microsoft Office Information Technology

Job description

  • Be familiar with, and work in accordance with, SOPs and Study Documents.
  • Complete all paperwork in compliance with good record keeping principles; correctly and on time in compliance with GLP/GCP and in accordance with Good Documentation Practices (GDP).
  • Prepare documents in accordance with requirements. Be able to effectively communicate findings and summaries from study data.
  • Utilize LIMS and other data systems to prepare data, chromatograms, tables, and figures for inclusion in reports.
  • Work with scientific teams regarding technical and study details.
  • Responsible for overseeing report lifecycle, addressing QA audits, and submission of reports to clients.
  • Be flexible; realise that timelines, priorities and requirements will change regularly and respond to these challenges accordingly.
  • Ability to plan and organise your work, while being aware of required timelines. Manage your own time and challenge yourself to identify and champion process improvement opportunities
  • Make suggestions for how processes can be improved and efficiency maximised, to include revising and/or creating report templates, lab manuals and other items as needed.

Requirements

  • BA/BS in a science or related field preferred; all experiences will be evaluated
  • Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP.
  • Demonstrated knowledge of scientific or technical writing, with proven written skills
  • Able to work in a regulated environment
  • Able to work effectively and contribute within a team
  • Able to work with computer systems; in-depth knowledge of Microsoft Office.
  • Able to document clearly

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