Clinical Evaluation Report Medical Writer – Contractor
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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