Our client is looking to fill the role of Medical Writer. The Contract Medical Writer is responsible for editing and performing quality control (QC) reviews of clinical procedures. This role will develop and revise clinical procedures. The Writer ensures that procedures, forms, and templates adhere to high-quality standards and the company's writing style guide, as well as standards for clinical procedures/documents. This is a 6 month contract role and is based in South San Francisco. Our employees follow a hybrid schedule of 4 days in the office, and 1 day remote. Responsibilities: Edit and perform QC reviews of clinical procedures. Work with Process Owners, SMEs, and stakeholders to develop and revise clinical procedures. Ensure that procedures, forms, and templates are written to a high-quality standard. Adhere to the company’s writing style guide and standards for clinical procedures/documents. Qualifications: 5 years of relevant experience Pharmaceutical or Biotechnology experience required Proven writing, editing, and quality control review experience. Experience in applying writing style guidelines and standards. Experience across multiple disciplines within clinical development in the pharmaceutical industry, with knowledge of the drug development process. Proven experience in developing, maintaining, and using electronic templates. Experience working in an electronic document management system. If you meet the required qualifications and are interested in this role, please apply today. #J-18808-Ljbffr Clinical Resource Network (CRN)
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