Marketing Operations Material Review Editor

A-Line Staffing Solutions

Job Description

Marketing Operations Material Review Editor openings in the Lake Forest / Mettawa, Illinois 60045 area with a major pharmaceutical company! Starting ASAP!! Apply now with Luke H. at A-Line!!!

Reason for opening: Expanding the role and need of the Material Review Process editors.

Description:

  • The Editor, Marketing Operations Material Review functions as editorial review for all advertising, promotion, disease awareness and promotional labeling material.
  • The Material Review Editor reviews assigned material throughout the review process to ensure quality, accuracy and conformance to company standards/guidelines.
  • Acts as content champion, collaborating with the review and brand teams to ensure changes requested are correctly incorporated prior to use and distribution.
  • Preferably on site/local but willing to consider off site/remote, but will need to vet this as we move forward; Home office work space is preferred, but during COVID, other considerations may be agreed upon by MO.

Pay Rate: $30 – $40 hourly (determined on experience)

Work Schedule: start between 7am-9am for a 40-hour work week Monday-Friday, (typically starting at 8:00 or 9:00, but do have some flexibility to adjust to individual considerations)

Top Skills Requirements:

  • Bachelor of Science or Bachelor's degree in English or Communications will be considered.
  • 5 years relevant pharmaceutical/healthcare industry experience in a related area such as medical writing, quality, regulatory clinical research, or product support/Research Development desired.
  • Advanced Microsoft Office Skills.
  • Experience with electronic document management systems.
  • Effective written and verbal communication skills, demonstrating proficiency in reading comprehension, grammar, and sentence structure
  • Ability to prioritize, multitask, and manage multiple jobs in a fast-paced, rapidly changing environment
  • Strong interpersonal skills with the ability to collaborate well with others and operate as a good team player

Why Apply:

  • Full benefits available after 90 days: Medical, Dental, Vision, Life, Short-term Disability
  • 401k after 1 year of employment: With employer match and profit sharing
  • GREAT Hours! Monday through Friday, 40 hours per week
  • Competitive Pay Rate!

Keywords: Marketing Operations, Marketing, Proofreading, Marketing Review, Material Operations, Operations Review, Editing, Editor, Operations Editor, Marketing Editor, Material Review, Material Review Editor, Regulatory Affairs, Regulatory Compliance, Arch Virtual Doc System, pharmaceutical industry, Quality Assurance, Clinical, Pharmaceutical, Quality Control, Medical Writing, Clinical Regulatory documents, regulatory clinical research, Trial Master File, TMF, ICH, GCP Guidelines.

Job Requirements


Top Skills Requirements:

  • Bachelor of Science or Bachelor's degree in English or Communications will be considered.
  • 5 years relevant pharmaceutical/healthcare industry experience in a related area such as medical writing, quality, regulatory clinical research, or product support/Research Development desired.
  • Advanced Microsoft Office Skills.
  • Experience with electronic document management systems.
  • Effective written and verbal communication skills, demonstrating proficiency in reading comprehension, grammar, and sentence structure
  • Ability to prioritize, multitask, and manage multiple jobs in a fast-paced, rapidly changing environment
  • Strong interpersonal skills with the ability to collaborate well with others and operate as a good team player

Keywords: Marketing Operations, Marketing, Proofreading, Marketing Review, Material Operations, Operations Review, Editing, Editor, Operations Editor, Marketing Editor, Material Review, Material Review Editor, Regulatory Affairs, Regulatory Compliance, Arch Virtual Doc System, pharmaceutical industry, Quality Assurance, Clinical, Pharmaceutical, Quality Control, Medical Writing, Clinical Regulatory documents, regulatory clinical research, Trial Master File, TMF, ICH, GCP Guidelines.

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