Freelance Writing Jobs : Spokane, Washington

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16
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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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22
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Johnson & Johnson - Spring House, PA - Director, Regulatory Medical Writing-5061150420 Description Janssen Biotech, Inc., a division of Johnson and Johnson’s family of companies, is currently recruiting for a Director, Regulatory Medical Writing for their Spring House, PA location. For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of individuals with serious disease. Built upon a rich legacy of innovative firsts, Janssen Biotech, Inc. pursues innovative... treatments, but also to new ways to empower patients and expand their access to quality care. For more about Janssen Biotech, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit www.janssenbiotech.com. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer . The Director, Regulatory Medical Writing will provide management in work assignments and oversight of approximately 4 direct...
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25
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Major Pharmaceutical Company - Deerfield, IL - Accountabilities: · Takes responsibility for medical writing operations activities (document preparation and/or production), including oversight of editorial and document support technician resources. · Provides organizational support and leadership support for Global Document Standards facilitating the review and approval of standards documents serving as primary liaison between TPC and functional areas in PDD. Oversees preparation of documents for regulatory submissions, ensuring... of contact for Global Project Subteams and Project Working Groups with regard to consistent interpretation and implementation of standards across programs. · Manages the editing and word processing subfunctions of Medical Writing; ensures consistency and efficiency in the production of documents that conform to PDD standards, provides leadership, and oversees recruitment of employees and contractors within the subfunctions. · Oversees the development and maintenance of Global Endnote reference management...
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26
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Sterling Life Sciences - Newark, NJ - regulatory documents br 8) Schedule and track all assigned medical writing activities in close cooperation with the teams to ensure high quality, timely, and accurate completion of all documents at each point in the document lifecycle br 9) Work with medical writing management for strategic planning, production & review of assigned summary documents br More questions? Want to know the Salary range? Keep reading. br/ br / The best way to get more details is to click ‘Apply’, upload your resume...Our client is currently seeking a driven and ambitious Manager, Medical Writing to join their team. This is a unique opportunity for a highly motivated professional who has a go-getter attitude. br br 1) Review work and manage activities for an entire program so as to contribute to successful completion of required program documents br 2) Provide intellectual leadership and contribute document knowledge and expertise to the global project team br 3) Manage the clinical development...
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International Pharmaceutical Company - West Chester, PA - Responsibilities ESSENTIAL AREAS OF RESPONSIBILITY: Manages and oversees a global team of Submission Ready Component (SRC) specialists Leads/manages the development of procedures/workflows for document creation and electronic publishing Assures adherence to global regulatory requirements and company guidelines as they pertain to electronic submission requirements Provides business administration support for all software used within global regulatory medical writing Coordinates/ trains... Three or more years of medical writing Functional Knowledge: World-wide government regulations pertaining to electronic submissions, specifically the electronic common technical document (eCTD). Regulatory documents in support of clinical research. Company/Industry Related Knowledge: Up–to-date with developments in the industry that impact on document management and electronic submissions. Demonstrated ability to work independently within an interdisciplinary, global team. Project management...
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Atlanta, GA - Job Responsibilities: Scope of Business Managed: Leads Business Insights analysis, reporting, and competitive intelligences and insights for all Writing Brands. Key interface with the Writing Segment Customer Development Organization to drive insights into action at the retailer level. Duties and Responsibilities: Develop understanding and expertise in the writing instrument category and leads cross functional team to develop best in class insights based on identification... of opportunities to enhance in-market performance. Analyze data and formulate conclusions about trends and practices in writing and other office supply product categories. Develop and present business updates for the internal organization. Proactively develop & provide Writing Segment Management with trends and analysis that guide business decisions Develop brand & merchandising strategies based on findings from customized shopper insights research, combined with marketplace data & consumer insights...
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Valmarc Corporation - Salem, NH - You need to have relational database experience, Linux environment, My SQL and or ORACLE, and extensive experience writing complex queries. I am seeking to identify a Database Engineer, US Citizen or Green Card, living within a reasonable commute to Salem NH. The key areas I am looking to identify in the successful candidate are listed below. Please take the time to review the details and in your response please help me to understand why you fit the required skill sets. Do you have 5...+ years of experience in relational database engineering, with at least 3 years using either MySQL and/or Oracle? Do you have extensive experience working on a LINUX platform? ( WE ARE NOT A MICROSOFT SHOP) Do you have experience writing and tuning complex SQL queries to extract data from highly normalized relational schemas? Do you have experience in creating solutions for processing our relational data collected and stored in RDBMS servers? Can you please tell us about your Relational...
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23
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Clemson, SC - and tutorial sessions); manage the Writing Center budget, in consultation with Center partners; lead Writing development programs (e.g., workshops); maintain and report annually on Writing Center statistics and records; mentor and advise the Assistant Director of the Writing Center; collaborate with faculty in Writing across the Curriculum and Writing in the Disciplines program; cooperate with the Pearce Center for Professional Communication; assess Writing Center results; and teach 2 English courses...The Department of English at Clemson University invites applications for Director of the Writing Center. With an Assistant Director and a staff of student tutors, the Writing Center supports writing instruction for students and faculty across Clemsons campus, in two on-campus locations and through one online portal. The Director reports to the Chair of and the Department of English, and, largely, will: interview, train, and supervise peer tutors; maintain the Writing Center schedules (staffing...
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26
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Not-For-Profit Science Advancement Organization - Holliston, MA - The Manager of Medical Writing serves as the lead Medical Writer on projects. As the lead Medical Writer, drafts and finalizes documents necessary for all phases of clinical drug and device development by organizing, analyzing, and interpreting scientific and statistical data. Such documents include, but are not limited to, clinical study reports, study protocols, investigator’s brochures, and manuscripts. Responsibilities include: Works with Project Manager to develop timelines and resource... plans for the production of clinical documents. Reviews statistical analysis plans and case report forms as required. Performs “peer” quality control (QC) review of clinical study reports and clinical sections of regulatory submissions written by other medical writers. Keeps management informed on progress of documents and other project related information, assists management in projecting resources, and performs administrative duties as requested. Documents are to be completed within a time...
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Johnson & Johnson - Raritan, NJ - Principal Medical Writing Scientist (Cardiovascular)-5094150408 Description Janssen Research & Development, LLC is recruiting for a Principal Medical Writing Scientist position, located in Raritan, NJ or Titusville, NJ or Spring House, PA. Janssen Research & Development, LLC develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes..., hematology, metabolic disorders, immunologic disorders, and reproductive medicine. This position will support the Cardiovascular therapeutic area. The Principal Medical Writing Scientist is responsible for preparing sound scientific/clinical documents in the Cardiovascular 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...
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