Freelance Writing Jobs : Alpharetta, Georgia

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26
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Houston Independent School District - Houston, TX - Hourly Lecturer (Writing Instruction/Intervention) JobID: 36236 Position Type: Closing Date: 11/23/2016 Instructional Support Staff/Hourly Lecturer Date Posted: 9/23/2016 Department: Hines-Caldwell Date Available: 09/23/2016 Location: Area: Job Category: Hines-Caldwell Southwest Paraprofessional, Administrative Support Staff Job Code: Contract Type: Months: H0077 None Salary Minimum: Salary Maximum: $15.56 $23.53 Description: Job Summary: Qualifications: Working...
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17
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Boston University - Boston, MA - The College of Arts & Sciences Writing Program at Boston University seeks an Associate Director for Writing in the Disciplines (WID) to lead a new WID initiative for Boston University, to begin July 1, 2017. The Associate Director for WID will also hold a non-tenure track faculty appointment as Professor or Associate Professor of the Practice in English or another appropriate department. Specific responsibilities will include: Developing an institutional strategy for supporting WID... at BU Advising other academic units on undergraduate writing and communication Organizing and leading professional development events for faculty Collaborating with other relevant units, such as the Educational Resource Center and Center for Teaching and Learning, to support faculty professional development and undergraduate education Contributing as appropriate to the administration of the Writing Program Pursuing an independent research agenda in writing/communication studies Teaching three classes...
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29
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California - A leading human therapeutics company in the biotechnology industry needs applicants for an opening for a Work at Home Regulatory Writing Manager in Thousand Oaks. Must be able to: Write or oversee the writing of clinical study reports Prepare and oversee the preparation of regulatory submission documents that comply with global regulatory standards Act as a functional area representative and lead on product teams Skills and Requirements Include: Ability to provide expertise and guidance... on document design and principles of good medical writing to the department and product teams Ability to assist with the following activities: hiring, resourcing therapeutic areas and project teams, and departmental governance Ability to ensure quality of regulatory submission documents at all stages of development Doctorate degree Ability to participate in departmental meetings, as well as departmental and cross-departmental initiatives, as appropriate...
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Yoh - Thousand Oaks, CA - to Bring to the Table: Technical writing experience for documents in a regulated environment Bachelor's Degree or Associates Degree with 4 years related experience or High School diploma/GED with 6 years related experience Bonus Points! Otherwise Known As Preferred Qualifications: Experience working with documents in a regulated industry Understanding of GMP requirements Ability to perform routine functions using established standards and procedures Ability to work independently...
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8
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Collegeville, PA - About Pfizer All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That's why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission of making the world a healthier place. Role Description *Associate Director, Medical Writing Author... questions from regulatory authorities. *The Associate Director, Medical Writing Author provides project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission. Provide project teams with expertise and strategic guidance on analysis and presentation of clinical and safety data and on benefit-risk assessment in documents. *Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In...
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Palo Alto, CA - The Associate Director is responsible for writing and managing the completion of a broad range of documents in support of company products and projects; will craft document messages and write, substantively rewrite, and edit documents for sense, clarity, accuracy, and effectiveness; will manage project documents, timelines, and contract writers; and will ensure that documents comply with ICH guidelines, Company SOPs, GCPs, and GPPs. This individual will work with colleagues companywide... to ensure that documents meet the company’s objectives and its high quality and compliance standards. Essential Functions Provide companywide writing and editing direction and support Write or substantively edit high-quality written documents, including investigator’s brochures, clinical study protocols and reports, integrated summaries, pre-meeting packages, requests for scientific advice, pediatric investigational plans, literature reviews, journal aCompanycles, SOPs, responses to regulatory...
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New Brunswick, NJ - . Required Knowledge, Skills, and Abilities Equipment Utilized Physical Demands and Work Environment Overview The Rutgers Writing Program provides instruction to over 14,000 undergraduate students yearly across all five Rutgers-New Brunswick campuses. We offer required writing classes and advanced courses in research, business, science, and technical writing, all of which prepare students to succeed throughout their academic careers at Rutgers and beyond. The Writing Program draws on full-time instructors...The nationally recognized Rutgers Writing Program welcomes applications year-round for the position of Part-Time Lecturer. Our faculty teach students to close read nonfiction prose, connect texts, synthesize ideas, and present independent arguments clearly with support from textual analysis. We invite you to apply to become a part of our growing community of writing instructors. Minimum Education and Experience MA required. PhD and/or university writing instruction preferred...
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General Dynamics UK Limited - Quantico, VA - Point Information and Content Management/Technical Writing SharePoint Information and Content Management/Technical Writing Requisition ID RW249843 # of Openings 1Job Location USA-VA-Quantico Job Function Information TechnologySecurity Clearance Level Secret More information about this job Job Description Job Responsibilities: 1. Provides application development and technical support for customer websites. 2. Collaborates with graphic artists to develop web page graphics that support interactive...
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Hewlett Packard - Corvallis, OR - Writing Systems Engineer Job Description:Join one of HP's most successful new enterprises, PWP, the HP PageWide Web Press organization. PWP designs, develops, installs, and supports HP digital web presses all over the world. These presses utilize the latest in HP proprietary inkjet technology. It is an exciting, fast-paced, and growing business. We are looking to hire a recent engineering graduate (degree from 2013-2016) into our Engineering Operations team in beautiful Corvallis, Oregon. The... person in this role will learn the web press writing systems in depth in order to solve complex printhead and/or press issues and improve the quality and reliability of our products for our customers. Responsibilities; Partner with experienced engineers to learn the press writing system and printing technology. Qualify ink and printhead design improvements. Respond to customer concerns about PQ and printhead issues. Investigate and determine causes of issues. Develop short term, immediate solutions...
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Pharmacyclics - Sunnyvale, CA - General Position Summary/Purpose: The medical writer will research, write, and edit clinical documents intended for regulatory submission, working with minimal supervision and managing all aspects of document development in a fast-paced, dynamic environment. In addition to managing multiple writing projects, the medical writer will represent Medical Writing on study teams and provide guidance to the teams on issues related to development of clinical regulatory documents. Essential skills... include the ability to develop clear, concise documents on tight timelines; demonstrated skill in writing from statistical output; an understanding of statistics, the principles of clinical research, the relevant regulations and guidelines, and AMA style; and careful attention to detail. Key Accountabilities/Core Job Responsibilities: • Research, write, and edit clinical documents intended for regulatory submission, working in multidisciplinary teams to develop documents that comply with relevant...
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