$55.00 - $55.00 / Hourly
40
1
Summary:
The purpose of this role is to write, or coordinate the preparation of, all clinical, regulatory and scientific documents intended to support clinical and regulatory deliverables for drug development project teams. The scope of the role includes authoring, review, and quality assurance check of documents, and management of external medical writers.
Project Details:
Author or coordinate the authoring of the following Clinical Documents: Study Protocols, Clinical Study Reports, Clinical Study Summaries (for posting to study registries) Author or coordinate the authoring of the following Regulatory Documents: Common Technical document (CTD) clinical and nonclinical sections for IND, NDA and MAA documents Briefing Documents for Regulatory Interactions, e.g., FDA Meetings, EMA Scientific Advice Responses to Regulatory Agency questions Author or coordinate the authoring of the following multidisciplinary documents: Investigator Brochure Orphan Drug Designation Requests Manuscripts and posters, including support for primary author, writing or coordinating first drafts, managing internal and external reviews and journal submission Manage external medical writing resources Organize Framework Meetings prior to the initiation of key clinical or regulatory documents to ensure alignment on essential insights and scope Coordinate the review and quality check of all documents Work with Clinical Development, Biostatistics, Safety, Regulatory Affairs and Project Management to ensure document preparation timelines are consistent with Program goals
Job Experience:
Five or more years experience in Medical Writing in the Biopharmaceutical industry, with experience supporting NDA filings Regulatory writing experience is preferred Ability to work without close supervision Direct management experience or experience coordinating external resources Excellent written and verbal communication skills Mastery of the English language, with a comprehensive understanding of English grammar and punctuation Ability to multi-task and complete assignments on time Excellent problem-solving capabilities and organizational skills Knowledge of medical, pharmaceutical, and clinical research concepts A high degree of familiarity with statistical and data output Expert level skills in relevant computer software including Microsoft Word, and familiarity with bibliographic citation tools and software Knowledge of the methods, techniques, and procedures of medical writing tasks Prior clinical protocol and CSR writing experience Prior experience with documents for submissions in electronic Common Technical Document (eCTD) format. Detailed and experienced-based understanding of applicable regulations, and the CTD structure.
Hourly Rate: 55-72
Oxford is an Equal Employment Opportunity Employer. All qualified applications will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Oxford will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. Oxford provides supplemental medical (we do not offer major medical), dental, vision, life, and disability benefit plans along with a 401(k) Retirement Savings Plan. Paid holidays based on eligibility and paid sick leave for applicable jurisdiction, as required. Oxford is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please email oxfordbenefitsgroup@oxfordcorp.com. We will make a determination on your request for reasonable accommodation on a case-by-case basis.
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254763-6804
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