Medical Writer II

Katalyst Healthcares and Life Sciences Boston, MA Open
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Katalyst Healthcares and Life Sciences is looking for Medical Writer II in Boston, MA.
This local job opportunity with ID 3662791708 is live since 2026-05-04 14:28:34.
Responsibilities:
  • Defines scope of quality control activities with the document author and the required source documents and data required.
  • Conducts independent quality control review of documents per applicable checklist by checking against source documents to ensure results are accurate.
  • Ensures quality control documentation is complete and accurate and uploaded to the master file per the established business processes.
  • Maintain strong knowledge of clinical regulatory documents requiring quality control review and business processes.
  • Interacts daily with medical writers and/or medical writing managers and interfaces/communicates with applicable cross-functional areas.
  • Communicates and provides deliverables to medical writers, medical writing managers, and others as applicable.
Requirements:
  • Bachelor's degree required.
  • Bachelor's degree in science, English, or Communication preferred.
  • 2-3 years in relevant industry experience in quality control/review of clinical regulatory documents or related experience in an area such as quality assurance, clinical research, drug development, medical writing, regulatory, or product support/R&D. Note: Higher education may compensate for years of experience. Years of experience may also compensate for lower education.
  • Excellent knowledge of organization and content of clinical documents and eCTD structure.
  • Knowledge of drug development and experience with Common Technical Document (CTD) content templates.
  • Excellent oral/written communication, interpersonal/organizational, analytical/critical thinking, and conflict management skills.
  • Superior attention to detail and ability to prioritize multiple tasks/projects.
  • Experience in working with collaborative cross functional teams.
  • Operates with limited oversight.
  • Prepares technical documents to support both domestic and international regulatory submissions.
  • Incorporates text, graphs, charts, tables and statistical analysis.
  • Proofreads, circulates, edits, assembles, inspects and duplicates product submissions.
  • Experience Level = 3-5 Years.
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