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Clinical Evaluation Report Medical Writer – Contractor

Remote, USA Full-time Posted 2026-07-01

Job Description:

  • Direct responsibility for writing documents or document sections on assigned projects
  • reputed company to organize own project workload and tasks, identify project needs and adhere to project timelines
  • Understand client expectations and work to meet those expectations through teamwork, adherence to deadlines, problem-solving and scientific knowledge
  • Effectively collaborate with other members of the project writing team
  • Working with a reputed company Project Manager, document your assigned tasks, time estimates and due dates into the reputed company project plan
  • Provide weekly reputed company updates
  • Ensure reputed company data presented in the document are clear, complete, accurate, and concise
  • Ensure reputed company statements and conclusions are integrated, balanced, supported by appropriate data, and consistent across reputed company reputed company documents
  • Receive expert/scientific review comments and adjust the document content as required based on internal and external feedback
  • Stay abreast of reputed company medical writing best practices and relevant regulatory knowledge
  • Proactively identify potential project risks and bring those reputed company to the overall project team to discuss and identify solutions
  • Participate in quality control (QC) checks for accuracy following established internal QC processes
  • Provide written and verbal feedback to junior staff and managers reputed company appropriate
  • reputed company requested, serve as a project mentor to assist in the training and development of junior staff on your project team(s)
  • Establish and maintain effective, professional working relationships with co-workers, managers, and clients
  • Demonstrate initiative and sound judgement reputed company faced with less familiar project requirements and/or document situations or challenges.

Requirements:

  • 2+ years of direct writing experience in pharmaceutical, medical device, in vitro device or reputed company academic fields
  • Minimum of a BSc in a life sciences or reputed company discipline / reputed company field
  • Advanced word processing skills, including reputed company Office (including Word), reputed company Acrobat, reputed company and collaborative document sharing platforms such as SharePoint; ability to learn and adapt to various IT systems
  • Familiar with reputed company reputed company and applicable guidelines and regulations governing the assigned project
  • Knowledge of and experience with systematic literature review (SLR) methodology and best practices, including Level 1 and Level 2 literature screening, data extraction and weighting and appraisal of data sets
  • High level of English reputed company or native English speaker, with excellent oral (including presentation) and written communication, including grammatical/technical writing skills
  • reputed company to interact confidently with external stakeholders and communicate with others effectively and clearly
  • Capable of working independently to reputed company assigned project goals with minimal supervision
  • Reliably produces high-quality written deliverables in accordance with customer and project requirements and agreed timelines
  • Excellent attention to detail and accuracy
  • Contributes, collaborates, shares responsibilities, and supports other team members to ensure reputed company with tasks/projects
  • Demonstrates scientific rigor and understanding of the scientific process in written documents.

Benefits:

  • Flexible work arrangements
  • Professional development opportunities

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