Freelance Writing Jobs : Mississippi

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28
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Grainger - Tempe, AZ - Mgr, Technical Writing Processes & Procedures - Customer Service Centers Date: Jan 5, 2021 Location: TEMPE, AZ, US, 85283-4475 Virtual Worker, IL, US, N/A WATERLOO, IA, US, 50701-9371 LAKE FOREST, IL, US, 60045-5201 JANESVILLE, WI, US, 53546-8729 Company: Grainger Businesses Grainger is a global leading broad line supplier of facilities maintenance products serving businesses and institutions. Our nearly 25,000 employees are driven to serve customers and the community in exceptional ways... * Demonstrated flexibility to adapt to shifting demands and competing priorities * Strong competence in the use of technology and software applications including SAP, SalesForce, Verint and Microsoft Office Suite * Ability to plan, organize and delegate work * Ability to influence with and without authority to achieve individual and team objectives * Travel required, up to 30%. Domestic and International Locations. Grainger is an Equal Opportunity / Affirmative Action employer. All qualified applicants...
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18
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Journalism Next - Denver, CO - Announcing the national Al Nakkula Police Writing Contest, recognizing outstanding law-enforcement reporting during 2020. First-place prize $2,000. Award recognition by the Denver Press Club. For details and instructions, Use Discount code JNN21 for 10% off your entry fee. Indicate you saw this position on JournalismNext.com when applying. Contact Information Journalism Dept, University of Colorado Boulder Lisa Guinther 1511 University Ave Boulder, CO 80309 United States Ph: 303...
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22
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USA - Medical Writing - Reviewer 100 remote Contract Department Clinical Services RESPONSIBILITIES The medical writing reviewer collaborates with members of cross-functional teams in the preparation of clinical documentation within agreed-upon timelines. The reviewer conducts a thorough review of the clinical documentation with respect to Good Clinical Practices (Google Cloud Platform) in order to maintain the highest level of quality and compliance. POSITION SUMMARY middot To perform tasks including... literature search, summarizing and analyzing data from clinical studies for medical devices middot Review of medical journals and technical reports middot Working closely with clinicians, researchers and other medical services personnel to provide information which is accurate and easy for others to understand RESPONSIBILITIES bull Reviews literature articles and extracts relevant information bull Highly knowledgeable and experienced in the regulatory medical writing process bull Suggests or identifies...
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Daiichi Sankyo, Inc. - Basking Ridge, NJ - authoring, contribute strategically and scientifically at the project and/or study team level, manage CROs and external writers for document quality, and develop medical writing timelines, processes, and working standards. The position may independently serve as primary author of complex clinical documents (e.g., pivotal Phase 3 protocols and reports) and lead BLA/MAA submission document development. The Director, Medical Writing will possess advanced knowledge of BLA/MAA submissions, document... management systems, relevant therapeutic areas, and other aspects of drug development (e.g., nonclinical, pharmacokinetics, biostatistics). Responsibilities: Provide leadership and establish strategies for document authoring to projects/study teams at the organization level; Plan and coordinate medical writing activities in collaboration with stakeholders within and across regions. Critically review documents produced by writers for scientific content and alignment with company position, clarity...
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The City University of New York (CUNY) - New York City, NY - to Teacher (LTT) Program at the CUNY School of Labor and Urban Studies is a program that provides support services to Paraprofessionals and United Federation of Teachers (UFT) members employed with the New York City Department of Education (NYCDOE) to pursue their education and advance their careers in teaching or other fields of study. LEAP to Teacher program seeks to hire a Writing Specialist to work with LTT students at Brooklyn College. Description: The LEAP to Teacher Writing Specialist reports... to the Director of Worker Education and Workforce Development. The Writing Specialist will assist the LEAP to Teacher students with academic writing and research and provide tutoring sessions and mini workshops. The Writing Specialist will work with assigned faculty members in class, facilitate writing groups during class sessions, meet with students individually and in small groups to lead students to a greater understanding of their writing, demonstrate how to identify and correct writing...
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29
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Texas A&M University - Galveston - Galveston, TX - Writing Consultants assist students writers at any stage in the writing life-cycle including outlining, revising, and editing. A Writing Consultant uses......
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21
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San Francisco, CA - Nektar is seeking an experienced Sr. Director, Medical Writing to join its Regulatory Affairs team. This position will lead and oversee the Regulatory Department writing activities for all development projects, ensuring the support of all regulatory submissions to Health Authorities (HA) (FDA, EMA, etc), from pre-IND to post-marketing activities, and most importantly marketing authorization applications (BLA, NDA, MAA, etc.) to help achieve Company goals. The Sr. Director is responsible... for the management, planning and direction of a team of medical writers, including contractors, to ensure high quality documents to meet HA requirements/guidelines and to meet project deadlines. Directs the writing, editing and coordination of the review of all key regulatory documents. Works collaboratively with cross-functional teams to support the preparation of regulatory and clinical documentation to global HAs. This role will also include strategic and operational leadership relative to the...
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26
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Precision Medicine Group - Chicago, IL - implementing medical writing processes and standards. Experience overseeing the work of contract writers. Strong planning and project management skills, along with initiative and ability to be productive with minimal supervision and minimal administrative support. Ability to travel, approximately 10% is required. Preferred: Advanced degree (MS/PhD) 7+ years of experience as a medical writer in the sponsor and/or CRO setting Oncology and/or hematological oncology Experience (especially protocol...Senior Manager, Medical Writing - Clinical Trial Services at Precision Medicine Group, LLC Senior Manager, Medical Writing - Clinical Trial Services Location: Chicago, Illinois US Job Id: 6525 Position Title: Senior Manager, Medical Writing External Description: The Senior Manager, Medical Writing will be responsible for writing, internal review, and QC of various clinical and regulatory documents and distributing work to agencies, as needed. The successful candidate will work...
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Newton, MA - This position reports to the Head of Regulatory Writing and works with cross-functional team to develop regulatory documents. This position is a hands-on writing position. RESPONSIBILITIES: Works with the Regulatory Lead to develop the overall strategy of regulatory documents. Authors regulatory documents such as meeting requests, briefing books, responses to Agencies, Clinical Overviews (Module 2.5), etc. Leads kick-off meetings for creating regulatory documents. Leads and manages... cross-functional teams to review drafts of documents. Leads roundtable discussions to help resolve comments from cross-functional team members. Ensures that documents adhere to ICH, FDA, EMA guidances. Ensures that documents are properly formatted. Coordinates the QC review of regulatory documents. Qualifications At least 5 years of Regulatory Writing experience. Must have a background in science and be able to interpret statistical outputs. Preference for advanced degree. Experienced in...
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Boston, MA - Head of Medical Writing, Rare Disease 1110094 Job Scope Purpose Our long-standing, rare-disease focused client is on the heels of their first approval and seeking a Head of Medical Writing to join their impressive team. Thus individual will fall in a Director or AD level in experience, and manage clinical and regulatory documents for multiple programs. This individual will oversee a team of external Medical Writers to ensure the effective management and timely execution of scientifically... accurate, informative, and persuasive documents for regulatory filings, with aligned messaging across documents. Primary Job Responsibilities Help develop messages and ensure consistency across clinical and regulatory documents. Serve as point person for communication between all writing vendors and internal teams. Proactively contribute to development and implementation of Medical Writing best practices and improvements leading to efficient systems, processes and tools for authoringreviewingediting...
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