Freelance Writing Jobs : Louisville, Kentucky

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Bethesda, MD - University (NIU) run Master's degree programs in support of the Department of Defense and Intelligence Community. Your work will support and manage the University's writing center. You will provide writing support to graduate students for course papers and Masters' thesis. Including managing the day to day operations of the writing center, responding to student needs, presenting workshops and tutorials on academic writing, and offering individualized and/or group consultation to students. If needed, the... ideal candidate must be comfortable teaching a research and methodology course. Your Responsibilities â?¢ Conduct individual consultations with students writing research papers, projects, and theses â?¢ Develop and deliver academic writing skills workshops/seminars for graduate and undergraduate students â?¢ Provide information on the writing center during new student orientation â?¢ Attend faculty and staff meetings/committees as required Your Qualifications â?¢ Strong writing skills and extensive experience...
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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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New Haven, CT - Position Summary This position is accountable for the timely preparation of high quality, regulatory-compliant clinical document deliverables for Alexion. This position will support the medical writing (WM) activities for one or more clinical programs. This position will function with moderate supervision. The scope of this position includes the writing, document management, and development support for clinical study-related documentation including, but not limited to, clinical study..., styles, and processes. Clinical document types include clinical study protocols, clinical study reports, Investigatorâ??s Brochures and updates, and other IND/CTA or global regulatory submission documents Supports development and implementation of strategy for writing and completion of high quality clinical documents Manages the writing and completion of documents and other assigned tasks within established timelines (editing and QC) and with highest quality in terms of scientific content...
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IDEA Public Schools Careers - Haltom City, TX - a powerful learning environment; plan and deliver purposeful, rigorous instruction; assess for mastery and track student progress toward goals; analyze data to intervene and adjust instruction; and seek excellence as an educator and an IDEA team member. Academy ELA content is state assessed in Texas in grades 3rd, 4th, 5th grades. Writing is state assessed in 4th grade. Responsibilities: Implement state learning standards and IDEA curricula and assessments to meet ambitious academic expectations...
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Emeryville, CA - The Director/Associate Director, Medical Writing is responsible for leading clinical regulatory medical writing activities for BeiGene that conform to domestic and/or international regulatory submission and internal document standards. Clinical regulatory documents include, but are not limited to, clinical study reports, clinical study protocols or amendments, investigator brochures, regulatory briefing documents, and clinical sections of INDs, NDAs, BLAs, MAAs and other regulatory submission... documents. This person will be responsible for the management, planning and direction of a team of full-time employees and/or contractors, consisting of medical writers, translators, and/or QC Specialists Essential Functions of the job: Manages clinical regulatory writing activities outlined in the clinical development plans across BeiGene, including those required to meet Corporate Goals. Works effectively with cross-functional groups ensure the production of high-quality, scientifically accurate...
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Merck & Co., Inc. - Rahway, NJ - Apply on Company Website Clinical Technical Editor, Medical Writing (Remote) Merck & Co., Inc. Rahway, NJ Posted 2 hours ago Apply on Company Website Job Description Our Clinical Research and Pharmacovigilance teams push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. The Medical Writing Department of the Global... Clinical Trial Operations (GCTO) organization prepares a variety of regulated documentation in for the clinical development portfolio. The Clinical Technical Editor (CTE) is a member of the Medical Writing team who is accountable for quality control of clinical documents intended for submission to regulatory agencies. In this role the CTE will: - Coordinate and perform our Company's Quality Control (QC) process for clinical documentation that includes, but is not limited to, clinical protocols...
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Edmonton, KY - Veja mais: english articles 1500 words, 1500 words operating system, article 1500 words, eassy writing makes good teacher 1500 words, writing bid......
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Medpace - Dallas, TX - Manager, Medical Writing Job Locations United States-TX-Dallas Category Medical Writing Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise... across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 40 countries. Job Summary Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Manager, Medical Writing to join our team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success...
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IKCON Technologies - Jersey City, NJ - IKCON TECHNOLOGIES INC delivers exceptional IT services and solutions that provide clients with definite edge over competitors and promoting highest standards of quality. We are currently looking for a [Medical Writing Contract Project Manager] with one of our clients in [UNKNOWN], [NJ]. If you are actively looking for opportunities, please send us your updated resume with your contact details. JOB TITLE Medical Writing Contract Project Manager CITY UNKNOWN STATE NJ TAX TERMS W2... EXPERIENCE 10+ Years INTERVIEW MODE Telephonic / Skype JOB DESCRIPTION The Medical Writing Project Manager is a member of the Medical Solutions Medical Affairs team and is responsible for the planning, development, writing and reviewing Post Market Surveillance Plans and Clinical Evaluation Reports to support Medical Solutions devices. Primary responsibilities include managing and writing Post Market Surveillance (PMS) Plans and Clinical Evaluation Reports (CERs) according to established...
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Vertex Pharmaceuticals - Boston, MA - interdisciplinary understanding, and integrates Medical Writing department activities with those of other departments. KEY RESPONSIBILITIES: Collaborate with key stakeholders to ensure understanding of program strategy and the nature of medical writing services required to deliver on program objective Proactively anticipate risks, solve complex problems, and seek out and implement process improvements Independently prepare clinical regulatory documents, including protocols, study reports, investigator...â??s brochures, and sections of regulatory submission Provide medical writing input for study designs and statistical analysis plans Thoroughly analyze and critically interpret data to determine the best approach to composing each document Provide expert-level input to cross-functional teams that work on standard operating procedures, process improvements, and integration of new tools and technologies Identify new technologies and initiatives related to the preparation of clinical documents, provide...
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