This is a paid freelance, remote position. As a worldwide leader, CBR operates at a rapid pace and is always looking for experienced and passionate contributors who can create original high-quality content in a timely manner. Write original features and lists that focus on TV (and streaming). Pitch article topics to our Editorial team. Be a dedicated and consistent contributor to the site. Follow CBR’s general Editorial Guidelines while producing unique and high-quality content. Produce articles in a timely manner to ensure that the latest industry news and most interesting content are always available to CBR’s loyal readers. Work under tight deadlines and submit tasks on time.

This is a paid freelance, remote position. As a worldwide leader, CBR operates at a rapid pace and is always looking for experienced and passionate contributors who can create original high-quality content in a timely manner. Write original features and lists that focus on movies (and streaming). Pitch article topics to our Editorial team. Be a dedicated and consistent contributor to the site. Follow CBR’s general Editorial Guidelines while producing unique and high-quality content. Produce articles in a timely manner to ensure that the latest industry news and most interesting content are always available to CBR’s loyal readers. Work under tight deadlines and submit tasks on time.

• Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. • Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. • Coordinates quality and editorial reviews. • Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format.

• Authoring and Quality Assurance of Project Activities • Executes project specific activities with high quality and in defined timelines according to standard processes and operating procedures • Marking /QC/Review and/or editing of pertinent documents such as Clinical study documents for regulatory submission • Protocol and results summaries to support clinical trial disclosure commitments • Systematically perform quality control checks of documents prepared by colleagues against checklist • Perform detailed analyses on a planned and ad hoc basis, relating to processes and their outputs • Completion of Internal and Client specific training • Assist in mentoring and training of team members