Freelance Writing Jobs : St. Augustine, Florida

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21
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American Medical Group Association - Philadelphia, PA - The University of the Sciences Biomedical Writing Program invites applications for the position of full-time Assistant Professor of Biomedical Writing (12-month, non-tenure track). This is an excellent opportunity to be part of the only Biomedical writing program in the US. Reporting to the Director, Biomedical Writing Programs,the programs are an MS in Biomedical Writing, Certificate in Regulatory Writing, Certificate in Marketing Writing. This position is responsible for: Teaching... Instructing courses in non-regulatory and regulatory medical writing for the pharmaceutical and health-care industries Instructing courses including at least one core course, and serve as mentor/advisor in at least one of the two capstone courses for a total of 9 credits per semester, 27 credits per year including SummerA semester Participate in course and program development Help in team teaching for an additional 2 credits per year if needed Service to the programs and the university Help program...
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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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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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25
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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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J&J Family of Companies - Titusville, NJ - service providers as needed. The successful candidate will mentor/train junior writers or other peers. Demonstrates excellent listening skills and is proficient at sending clear, convincing, and well-tuned messages through a variety of media including but not limited to business discussions and agreements (one-on-one or larger groups) and electronic mail messages. The Principal Medical Writing Scientist will be able to negotiate with and influence others with regard to scientific content and process...** 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...
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Major Pharmaceutical Company - Gaithersburg, MD - cross-functional and cross-project learning across the organization. Contributes substantially to the MC vision and purpose, merging technical and business strategies, plans, and actions. *Collaboration: Interacts and collaborates with other functional area heads across Clinical Biologics, R&D, and to ensure department alignment, deliver workgroup solutions, and lead organizational change. Position: 10+ years experience in the medical/regulatory writing field in a pharmaceutical/biotech... industry or CRO environment in positions with increasing levels of responsibility. Includes proficiency at authoring/editing and managing the writing/review of multiple types of clinical regulatory documents and submissions. Background in biologics a plus. *3+ years of supervisory experience for multiple direct reports or contract staff in a medical writing/communication group or equivalent. *Broad cross-functional understanding of the drug development process from scientific, technical and business...
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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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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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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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Horizontal Integration - Denver, CO - , as well as other miscellaneous communications needs. Strong writing, editing, page layout, and production skills are required, along with an aptitude for integrating information from multiple sources. Position may require travel in support of marketing/education events or congresses with target audiences. All activities must be performed in compliance with the Quality System. Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations EDUCATION...
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