Document Quality Reviewer II

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Job title: Document Quality Reviewer II

Company: Parexel

Job description: The Document Quality Reviewer (DQR) II will conduct document quality review of medical writing deliverables and ensure timely delivery of error-free, high-quality clinical documents by correcting errors in grammar, style, syntax, and format ensuring

The Document Quality Reviewer (DQR) II will conduct document quality review of medical writing deliverables and ensure timely delivery of error-free, high-quality clinical documents by correcting errors in grammar, style, syntax, and format ensuring accuracy of the clinical data and content presented, identifying and fixing flaws in logic and flow, and following appropriate style guides/templates. The DQR II will independently provide editing support for more complex clinical documentation. Reports To: Department Line Management, Medical Writing Services Directly Supervises: None Provides Work Direction to: Junior Document Quality Reviewers Works Closely with: Medical Writing staff External Relationships: Client representatives Key Accountabilities: Ensure that all work is complete and of high-quality. Edit clinical documents by checking language, grammar, technical terminology, accuracy of data and scientific content. Confirm consistency and integrity across the document. Perform format changes to documents based on guidelines. Ensure that the document adheres to specified style guides or client conventions. Independently perform quality review of clinical components of assigned documents (e.g. patient narratives, informed consent forms, disclosure documents, protocols, clinical study reports, investigator brochures, summary documents, regulatory responses, etc.). Formally document quality review findings for assigned documents using department specific procedures. Identify and immediately escalate any significant findings. Qualifications Education: Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent. Knowledge and Experience: Experience in the pharmaceutical or clinical research organization industry and medical writing. Knowledge of regulatory documents and ICH-GCP guidelines, understanding of clinical research, and the drug development process. Proof reading, quality control and copyediting experience. Advanced word processing skills, including MS Office software and systems knowledge or ability to learn and adapt to various IT systems document management systems, collaborative authoring and file conversion and databases. Experience of safety aggregate reports a distinct advantage. Skills: Impeccable written and verbal communication skills and strong command of the English language. Ability to deliver consistently high-quality output. Well-established proof-reading skills and ability to pay rigorous attention to detail. Demonstrate excellent interpersonal skills and proactivity. Take initiative and work in a solutions-driven manner. High level of numeracy, ability to interpret statistical data and an understanding of clinical research concepts would be an advantage. Client-focused approach to work. A flexible attitude with respect to work assignments and new learning. Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail. Willingness to work in a matrix environment and to value the importance of teamwork.

Expected salary:

Location: Bangalore, Karnataka

Job date: Wed, 20 Jul 2022 22:57:12 GMT

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