Freelance Writing Jobs : Bromley

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Specialty Biopharmaceutical Company - Lexington, MA - Primary Duties The Medical Writing Group Lead (Dir) is responsible for strategically planning and resourcing the medical writing deliverables that support business objectives across a large therapeutic program or multiple programs. The MW Group Lead independently provides strategic direction to cross-functional project teams to ensure that clinical documents (eg, investigators’ brochures, study protocol and amendments, study reports, marketing authorization submission documents) accurately... Group Lead initiates and leads initiatives designed to establish best practices and efficient cross-functional collaboration. The MW Group Lead has direct people management responsibility including performance management, skill development, and fostering a BRAVE culture. In addition, may be responsible for budget and resource allocation pertaining to MW activity. The MW Group Lead reports to the Head of Medical Writing. Responsibilities 35% Writing, most often the more strategic documents...
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For-Profit Educational Organisation - Phoenix, AZ - to ensure students success. This position is accountable for the overall team management and ensures the quality and integrity of the college’s full-time faculty programs. The position requires a master’s from a regionally accredited college or university; a doctorate is preferred. Five years of teaching experience is required. Prefer candidates that have experience teleworking and or experience supervising teleworkers. The ideal candidate will have experience teaching Academic Writing at the... and technical knowledge of the curricula by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies. This includes maintaining a general knowledge of emerging issues and trends related to the respective campus Academic Affairs program(s). Results oriented and able to organize and independently manage various projects or processes simultaneously. Some travel may be required. Performs other duties as assigned...
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Cheshire, CT - supervision. Manages the writing and completion of documents and other assigned tasks within established timelines (editing and QC) and with highest quality in terms of scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines, styles, and processes. Actively supports clinical project team(s), representing Medical Writing and takes responsibility for timely and accurate MW deliverables, negotiating timelines as necessary. Participates... with other medical writing team members to formulate writing strategies and standards to be implemented and takes responsibility for execution. Develops effective collaborations with other functional lines in , and externally with regulatory, industry, professional, and academic organizations Ensures consistent support and implementation of medical writing standards Reviews, edits, and ensures quality of documents or sections of documents prepared by other writers (internal or contractors) or functional area...
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Sterling Life Sciences - Seattle, WA - A brilliant opportunity exists for an outstanding individual capable of fitting in to this very rewarding Senior Director of Medical Writing role. Our client is looking to hire someone who can bring in additional value to the role; so if you're someone who is dedicated, energetic and can ensure thorough attention to detail at all times, this could be the perfect role for you. br br 1) Provide medical writing support to Clinical Development and Regulatory Affairs br 2) Work closely... across all functions to ensure adequate medical writing support with timely delivery of quality clinical, regulatory documents and other documents br 3) Work closely with project team members to ensure that protocols, clinical trial reports, investigator brochures, IND reports, NDAs, sNDAs, orphan drug applications, post-marketing reports and international regulatory filings are accurate, and prepared in accordance with the appropriate regulations and guidelines br 4) Ensure that documents are appropriately...
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FLUCON - Peabody, MA - Ghost writer to write a book on leadership based on the theme and ideas that I have.Preferably able to work for 1 month starting 25th May and complete about 150 pages ghost writing.The expected writer can be a PhD student or an experienced one but really good at expression and easy with words.Fees for the work will be happily paid and can be decided upon meeting.Looking for some writer from Boston-Cambridge so that frequent personal interaction will be possible.-Sanjay Inamdar...
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Owego, NY - Lockheed Martin Corporation Owego, NY Description A technical writer shall be an expert author who is able to create clear, concise, compelling descriptive narrative for inclusion in competitive proposal offerings. This form of writing generally focuses on creation and organization of explanatory content for proposals and white papers. The technical writer has sufficient familiarity with the subject area that they understand the general principles of operation and use of relevant products... narrative. Strong command of the English language and grammar. Ability to work with graphic artists to create compelling proposal graphics. Ability to work flexible schedule to meet strict writing deadlines. Proficiency with Microsoft Office Desired skills Experience writing technical proposal content in response to RFI''s/RFP''s for the federal government; DoD proposal writing experience. Working knowledge of SharePoint. As a leading technology innovation company, Lockheed Martins team of 113,000...
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Teva Pharmaceuticals - West Chester, PA - Please Enable Cookies to Continue Please enable cookies in your browser to experience all the personalized features of this site, including the ability to apply for a job. Non Clinical Writing Specialist Requisition # 15-14485 # Positions 1 Location US-PA-West Chester Experience (Years) .. Category Research & Development - Pharmaceutical Do YOU have great ideas? Want to work in an environment that will nurture your professional development? Come and join Teva on its journey.... Their skills and dedication make us an industry leader. The diversity of perceptions, qualifications and talent are the key to our ongoing accomplishments. We offer a wide range of jobs and genuine opportunities for personal and professional advancement. More information about this job Overview The Nonclinical writing Specialist is responsible for writing and documentation work associated with nonclinical submissions in line with applicable regulatory requirements and Teva SOP. Responsibilities...
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CCCU - Azusa, CA - Azusa Pacific University is a comprehensive, evangelical, Christian university located 26 miles northeast of Los Angeles, California. A leader in the Council for Christian Colleges & Universities, APU is committed to excellence in higher education. Offering over 80 bachelor’s, master’s and doctoral programs on campus, online, and at seven regional centers across Southern California, APU has been recognized as one of U.S.News & World Report's Best Colleges for seven years running.... Description: The Director of the Writing Center administers all aspects of the Writing Center, which serves traditional undergraduate, graduate, and non-traditional students. The director provides leadership for and coordination of writing tutoring for students across the university’s multiple campuses; provides students with structured, personalized writing instruction that reflects and integrates current writing theory and practice for a wide range of writing projects including thesis and dissertation...
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Johnson & Johnson - Titusville, NJ - Principal Medical Writing Scientist-00000Y55 Description Janssen Research & Development, LLC is recruiting for a Principal Medical Writing Scientist position, located in Raritan or Titusville, NJ, Springhouse, PA, Fremont, CA or High Wycombe, UK or Beerse, Belgium. This position will support the Neuroscience therapeutic area. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing... inspire us. We collaborate with the world for the health of everyone in it. The Principal Medical Writing Scientist is responsible for preparing sound scientific/clinical documents in the neuroscience area under minimal supervision using established templates and guidelines. This person prepares and finalizes basic and complex clinical documents with increasing independence. Documents must be of high quality in terms of scientific content, as well as organization per regulatory and internal...
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Lexington, MA - Primary Duties The Head of Medical Writing provides senior leadership and coordination of all medical writing activities across multiple projects across all programs. Responsible for strategic planning of medical writing deliverables and provides strategic direction to clinical and cross-functional project teams relative to consistency of key messages across documents in concordance with program goals and regulatory requirements/guidance. Ensures timely preparation of all clinical regulatory... or contractors) as required for timely high quality clinical regulatory submissions. Initiates and leads efforts for establishing departmental guidelines, process improvements, and cross-functional initiatives. Responsibilities 50% Responsible for all medical writing management across all clinical programs including strategic planning of MW deliverables, negotiating timelines, risk mitigation, managing and coordination of resources (writers, editors, and clinical publishers [internal or contractors...
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