Freelance Writing Jobs : Kentucky

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22
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Boehringer Ingelheim - Ridgefield, CT - Description: Executes medical writing activities for projects in accordance with applicable regulatory regulations and Boehringer-Ingelheim requirements under the supervision of the Sr. Associate Director or Director of Medical Writing. Assumes primary responsibility for preparation of documents supporting major regulatory submissions and other documents as assigned, and assists the manager in coordinating and evaluating the activities of other contributors (including contract writers... Ingelheim's high regard for our employees. Duties & Responsibilities: Contributes to development of global regulatory documentation strategy and execution of tactics. Conceptualizes and develops medical communications for message-driven, concise reviewer-friendly clinical documents in order to support regulatory agency review. Coordinates medical writing/regulatory submission progress against global regulatory strategic communication plans. Writes or co-ordinates writing and reviews of clinical...
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Precision for Medicine - Flemington, NJ - 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 closely with cross-functional teams to ensure these documents are of high quality and completed in a timely fashion compliant with SOPs, ICH/GCP/regulatory guidelines and eCTD requirements. In addition, the successful candidate will be responsible for managing employees... and resourcing within the Medical Writing Department. Essential functions of the job include but are not limited to: * Planning, writing, editing, reviewing, and/or collaborating on development of timely and high-quality clinical and regulatory documents (e.g., protocols, investigator brochures, clinical study reports, patient narratives, annual safety reports, INDs, eCTD/NDA clinical summaries, briefing books). * Efficient review and finalization for documents produced internally and/ or externally...
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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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TransPerfect - Durham, NC - The Project Manager, Medical Writing (PM) is the main point of contact for clients at TransPerfect. The PM will be responsible for day to day project management and oversight of medical writing projects, and will be in daily and regular contact with clients. The PM will also be responsible for keeping up- to-date SOPs regarding medical writing processes. The PM will be required to meet all client timelines and work in conjunction with the medical writing manager, medical writers, and account... managers, and will be accountable for the success of all medical writing projects. This role reports directly to the Group Manager of TransPerfect s Medical Writing division. Responsibilities_include,_but_are_not_limited_to: * Oversee all elements of medical writing projects, and set and fulfill client expectations * Oversee project budgets and monitor costs against Client Budget and Statement of Work * Monitor and communicate project progress, ensure strict adherence to deadlines and budgets...
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Newell Brands - Bentonville, AR - This position is based in Bentonville, AR working with the Writing Business Unit Walmart team, and reports to the Director of Sales. Job Summary: This role is responsible for sales support coordination and data analysis by leading key processes, providing reporting and analysis, and looking for ways to streamline and improve current processes. This role will interact with many groups across the Sales and Sales Planning organizations and be responsible for coordinating and running key... meetings with relevant people and teams. Job Responsibilities: Sales / Operational Support Own QMS (New Item) & Sample process for Writing team, supporting Account Managers Maintain Feature Planning Coordination and reporting, working with Account Managers, Sales Planning, and Demand Planning teams to plan and communicate accurate details Support Account Managers with Feature Performance/Sell-through Analysis for all features Lead UL/CTL Product Testing process to maintain up-to-date standing...
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CyberCoders - Irvine, CA - will be considered. In addition to that, - Minimum 3-5 years Geotechnical Writing Experience - Live within the Los Angeles/Orange County area - M.A. Geotechnical and has a P.E. For the Mid-level Geotechnical Engineering position, you need: -P.E. License w/ 3 years of writing experience For the Senior-level position, you need: -P.E. (with the intent to get a G.E. soon)What's In It for You - Medical - Dental - Relocation - 401k: Profit SharingSo, if you are a Geotechnical Engineer with experience, please apply today!...
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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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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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Syracuse University - Syracuse, NY - The Department of African American Studies at Syracuse University seeks a part-time instructor to teach AAS 138: Writing About Black Culture for 3 credits at the undergraduate level in the Spring 2021 semester. One candidate may be hired to teach two sections: M001-Tu/Thurs-3:45-5:05 pm and M002-Tu/Thurs-2:00-3:20 pm. This course is designed to teach expository writing based on cogent analysis of African American literature, art, music, and historical ideas. In this process, students... will be focusing on acquiring information, improving writing skills and sharpening critical thinking ability....
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