Freelance Writing Jobs : Alpharetta, Georgia

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Enquizit Inc - McLean, VA - Technical Proposal writing, RFP, Federal, proof reading, Agile, Cloud and OpenSource Technologies. Preferred Skills : Domain : Work Authorization US Citizen GC EAD (OPT/CPT/GC/H4) H1B...
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29
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San Francisco, CA - Leading Pharmaceutical / Biotech Company Consulting is looking for a Clinical Regulatory Writing SME to join our Integrated Product Development (IPD) Team. Our IPD Team provides clients with the strategies and services around defining and executing the most efficient path to obtaining regulatory approval. A Senior Consultant within IPD must have a comprehensive understanding of the organization’s consulting models and methodologies, as well as, profound knowledge within a business context..., results or team performance and proactively takes action Leverages information from previous projects or other client work to complete assigned project activities as well as facilitate business decisions Produces quality work that meets the expectations of PC (Leading Pharmaceutical / Biotech Company Consulting) and the client. Reviews the work of colleagues for content and quality to ensure the expectations of the client and PC are met Manages small projects and may manage larger project...
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ISN Corporation - Gaithersburg, MD - Design or suggest graphics for written proposal material Review and contribute to proposal outlines and compliance matrices Participate in content review sessions Review and edit final text for grammar, tone, style, clarity, and consistency Participates in advancing drafts throughout the writing process Incorporates appropriate comments in collaboration with lead(s), SMEs, and proposal management Supports final proposal production as required May write, review, and/or edit other corporate... documents as requested. Qualifications: Bachelor’s degree in English or other related discipline Minimum 3 years’ experience writing and editing Federal Government proposals and marketing materials Experience writing reports, briefs, and similar content Knowledge of the Federal Government’s acquisition process Strong knowledge of Microsoft Word, PowerPoint and Adobe Acrobat Experience using GovWin & FedBizOpps Ability to work under tight deadlines and on multiple documents Highly organized...
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14
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Amgen - Thousand Oaks, CA - congresses and writing meeting summaries; preparing or editing documents for internal use or for submission to external, regulatory bodies; providing strategic input to publication teams and congress planning teams; overseeing the work of publication vendors; contributing to internal, process improvement initiatives. This role provides an exceptional opportunity to be an integral member of a dynamic team that communicates the results of Amgen's research to the scientific community and embraces Amgen...
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29
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Hyde Park, NY - POSITION SUMMARY Culinary Institute of America adjunct faculty members are responsible for teaching students high standard of professionalism. The responsibilities of the position include but are not limited to: teaching and evaluating students. Adjunct faculty members also maintain office hours, assist students who are having difficulty with studies, and honor college policies. COLLEGE WRITING (ENGL-120) Students will write and revise essays that demonstrate their ability to read... and other duties as assigned. REQUIRED QUALIFICATIONS Education: Masters Degree in Writing, English or another related field PREFERRED QUALIFICATIONS PhD in area specialization Experience with Moodle or similar education software 1 year college level teaching experience REQUIRED SKILLS Strong interpersonal skills; excellent verbal and written communication skills; ability to effectively work with multiple teams across the organization. Ability to use sound judgment and discretion in handling...
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Los Angeles, CA - New York City, NY - Autobiography about my life from a kid growing up in Pontiac Michigan to living out a dream of becoming a marine to leaving a dream and starting over and becoming a business owner. IMG_1390.PNG Family I'm the one on the left...
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Thousand Oaks, CA - Job responsibilities include: Prepare and oversee the preparation of regulatory submission documents that comply with global regulatory standards Write or oversee the writing of clinical study reports and Investigator Brochures for products in all phases of clinical development (phase 1 through 4) Write CTD sections including the Summary of Clinical Efficacy, Summary of Clinical Safety, Summary of Clinical Pharmacology, Summary of Biopharmaceutics, Clinical Overview, Table of All Studies... at all stages of development Provide expertise and guidance on document design and principles of good medical writing to the department and product teams Participate in departmental meetings, as well as departmental and cross-departmental initiatives Basic Qualifications Doctorate degree OR Master’s degree and 3 years of Writing Regulatory or scientific submission/documents experience OR Bachelor’s degree and 5 years of Writing Regulatory or scientific submission/documents experience...
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Boston, MA - Overview: Oversees deliverables, supervises employees, and provides expertise in the area of regulatory writing, publications writing, and regulatory publishing. Responsibilities: Interviews and selects team members according to sponsor needs. Takes a lead role in the development of department procedures and initiatives. Collaborates with other departments to identify, investigate, and implement new business opportunities. Provides strategic direction for regulatory writing, publication... writing, or regulatory publishing programs. Qualifications : 5 years of leadership experience in clinical and scientific communications, including 2 years of formal people management experience Bachelor’s degree required. Advanced degree strongly preferred...
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Cambridge, MA - Job Summary: The Manager, Medical Writing is a key member of the Medical Writing team. The Manager, Medical Writing is responsible for the development and management of medical writing deliverables that support the clinical portfolio. Duties & Responsibilities: In this role, the Manager, Medical Writing: Works with project teams to prepare clinical and regulatory documents, including protocols, study reports, investigator brochures, INDs/IMPDs, and CTDs according to company and agency... Overview) to support high-quality submission dossiers. Ensures a consistent style of presentation of clinical document to maintain quality and ease of review, and adherence to company standards. Works effectively with company document management system and related tools, templates, and procedures in order to ensure efficient publishing of documents and dossiers. Mentors more junior medical writers and provides leadership in completion of large writing projects. Qualifications Bachelors’ degree...
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Billerica, MA - Who You Are: The Medical Writing Lead will be a core member of the Clinical Operations Team (COT), to serve as primary point of contact for the Clinical Operations Team on medical writing deliverables and to provide advice on Medical Writing issues to Global Project Team members and help to resolve problems. The Medical Writing Lead will also be responsible for writing strategic submission documents (e.g., IND, briefing books, ISS, ISE) and enabling regulatory submissions for Leading... Biopharmaceutical Company programs. The Medical Writing Lead will provide project management expertise working with CRO medical writers, key decision makers and internal team members to manage continuous process improvements, issue escalation, workload projections and provide technical expertise. The Medical Writing Lead will partner and work cross functionally internally with: Other GCO functions; Global Regulatory Affairs; Drug Safety; GDM Clinical Development Center; Non Clinical Development; Global...
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