Freelance Writing Jobs : Wilmington, North Carolina

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27
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Livermore, CA - REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES: MUST meet one of the numbered pathways below, as well as any applicable clarifications stated, (including education, area of study and previous work experience, including minimum number of years and types of experience): (1) Master’s degree or higher in English/Technical Writing or an equivalent discipline. (2) Masters degree or higher in any area and minimum of 18 graduate credits with a focus in English/Technical Writing. (3) Master’s degree or higher in any area... to: Composition and/or Rhetoric. Progressive experience working in the area of Technical Writing. Examples may include but are not limited to: College Faculty with related and active research agenda; Author, Writer, Technical Writer, Editor, and/or Technical Communication....
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27
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New Mexico State University - Carlsbad, NM - institution by the federal government with a total minority enrollment over 48%. Home to the state’s NASA Space Grant Program, NMSU is located in Las Cruces, which features desert mesas, the farmlands of the Rio Grande Valley, and the Organ Mountains, an extension of the Rocky Mountain chain. The University is committed to building a cultural diverse educational environment. Job Duties and Responsibilities Tutors work from 10 to 29 hours a week in an academic tutoring center as a writing tutor. Tutors... are required to work varying hours between 8 am to 6 pm Monday through Thursday. Required Education High School diploma or GED certificate. Required Experience Two (2) years of experience related to the standard duties as outlined. Classification Summary Provides academic tutoring services to a wide variety of individuals and groups. May work on an on-call, short-duration basis. Creates and implements tutorial programs that guide and assist students with homework, problem solving, report writing, and test...
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28
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Cambridge, MA - OBJECTIVES: We have a challenging opportunity for an Associate Director/Director, Non Clinical writing group based in Cambridge, MA, reporting to the Senior Director, Global DMPK head of Strategy and Operations. The candidate provides global non clinical writing group strategic direction and leadership and scientific writing content expertise for multiple compounds and/or projects within a therapeutic area. In this leadership role the candidate will be responsible for developing... and implementing global non clinical writing strategies, operational plans and innovative solutions for all non clinical writing activities. Interfaces with external groups (eg. GDMPK, Toxicology, Pharmacology, Regulatory, Clinical, Publishing) to ensure accurate and timely completion/delivery of information and review of non clinical regulatory submissions. Contributes to therapeutic area project teams as the non clinical writing expert for all regulatory submission documents. ACCOUNTABILITIES: Major...
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Princeton, NJ - The Senior Director or Director of Medical Writing is a leadership role that will be responsible for developing and implementing medical writing strategies, operational plans and innovative solutions for all medical writing activities. Lead both a small in-house and a large outsourced medical writing team in the delivery of high quality regulatory writing services in accordance with applicable regulations and internal requirements in support of multiple therapeutic areas and functions. These... services include document: Preparation e.g. CSRs, integrated summary documents, IBs, Health Authority meeting packages, annual reports, protocols, narratives etc. Quality control Use of document management system, internal style guide and templates A very key aspect is the development and integration of new technologies into Medical Writing. New technologies include the semi-automatic generation of document component text, specifically involving content reuse in automated CSR and narrative writing...
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29
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Princeton University - Princeton, NJ - Overview The Associate Director provides intellectual and administrative leadership for the Writing Seminars—small, intensive courses in academic inquiry and argument required of all of Princeton's more than 1,300 freshmen. Each year, the Princeton Writing Program offers ~112 interdisciplinary seminars on topics ranging from scientific breakthroughs and historical controversies to artistic traditions and social issues. Writing Seminar enrollment is capped at 12 students to allow... for frequent written and in-person feedback from faculty on student drafts and revisions. The ~35 members of the Writing Seminar faculty typically hold the Ph.D. and come from a range of fields in the humanities, social sciences, and natural sciences. The Associate Director’s primary responsibilities are to supervise the hiring, training, development, and assessment of faculty, and to ensure the effectiveness of the seminars through ongoing curricular enhancements that reflect recent advances in writing...
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AbbVie - USA - This position may be filled as a Medical Writing Coordinator or Senior Medical Writing Coordinator based on candidate's experience. The Medical Writing Coordinator/Senior Medical Writing Coordinator is responsible for providing regulatory document support to the medical writing teams, ensuring successful preparation of high quality submission-ready documents. Provides expertise in the management and coordination of casebooks, and other appendix 16 documents ensuring timely completion... more junior Medical Writing Coordinators. Participates in process improvement activities. Key Responsibilities Include: Implements selected activities (such as document workflows, tracking, and electronic QC) associated with electronic document-related activities for regulatory documents. Communicates deliverables, electronic document process, and durations associated with these activities to the Medical Writing Manager, Clinical Project Management, and other functional areas such as Publishing...
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Amgen - Thousand Oaks, CA - Amgen is seeking a Medical Writing Manager for their Scientific Affairs Cardiovascular therapeutic area. This is a full-time, Thousand Oaks, CA corporate office-based position. Amgen's Scientific Affairs medical writers work closely with opinion leader authors to develop manuscripts and review articles for peer-reviewed clinical journals as well as abstracts, posters, and slide presentations for scientific congresses. Consider joining a team that participates in developing and communicating... a Global Health Economics (GHE) value-evidence strategy for an Amgen pipeline asset or a Marketed Product. Global Medical Writing supports the GHE team in ensuring patient and payer perspectives are incorporated into the value generated for Amgen s innovative biologics. In addition to providing strategic input to product publication teams and scientific congress planning teams, Scientific Affairs writers liaise with medical leads, biostatisticians, and health economists as well as external opinion...
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Pharmacyclics - Sunnyvale, CA - Job Description: 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...
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King of Prussia, PA - /revises standards for GSK submission documents. Shows ability to identify and clarify problems, recommend creative solutions and influence appropriate changes to achieve desired outcomes. In addition, the Respiratory Medical Writing Manager: Provides significant contribution to complex clinical submission documents, including briefing documents and responses to regulatory questions. Acts as lead author/manager on submissions. Possesses thorough knowledge of major country regulatory requirements...GlaxoSmithKline King of Prussia, PA Description Basic qualifications: Bachelor degree in sciences Good working knowledge of ICH guidelines for Common Technical Document and Good Clinical Practice, FDA Code of Federal Regulations for New Drug Applications, European requirements for Marketing Authorization Applications, and other regulations governing clinical research and documentation. Proven track record in writing clinical documents including, but not limited to: clinical study...
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San Diego, CA - across groups and departments Good communication skills in writing and speaking Self-starter and strong initiative Highly Desired: Candidates should have completed their junior year by the time they begin internship Summer of 2017 Experience with controllers, debugging systems, programming devices Enthusiastic learner and creative thinker...
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