Freelance Report Writing Jobs : Albuquerque, New Mexico

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Bimbo Bakeries - Chicago, IL - area, for example: definition of goals, evaluation of goals, etc. Support the team in administrative tasks. Comply with global and local functional policies. Job Requirements A Bachelor's degree in Accounting, Finance or Engineering. A combination of education, training and experience that results in demonstrated competency to perform the work may be substituted. 1-2 years of experience in areas related to auditing. Basic knowledge in supply chain process such as procurement...®, Entenmann's®, Arnold®, Brownberry®, Oroweat®, Sara Lee® and more. Become one of the 20,000 associates who come to work with passion and dedication to their careers. More Jobs from Bimbo Bakeries USA Internal Auditor Houston, Texas, United States 22 hours ago Senior Internal Auditor Horsham, Pennsylvania, United States 22 hours ago Jobs You May Like Lead/Senior Auditor (1099/Freelance) - 40 hours... Paro Chicago, IL, United States Staff Auditor (1099/Freelance) - 40 hours per week...
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Computer Arts, Inc. - Meridian, ID - problems and provide solutions 2 years of SQL experience 3 years Crystal Reports Desired Requirements: Experience with querying datasets, writing stored procedures and SQL language experience Experience with basic programming and system analysis procedures is preferred Experience with sub-reports and data grouping Experience with local government departments, accounting and XML a plus! We offer a competitive salary and excellent benefits. Send resume to Karolyn Reid at ....
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Greene Resources - Raleigh, NC - Job Description Job Number: 41015 Copy Editor Job Description: Our client is seeking several Copy Editors with excellent editorial, reading, writing, and organizational skills to be part of their growing team. You?ll be responsible for delivering publication-ready content that is on-time, fully optimized for SEO and meets their marketing goals. You also enjoy writing; you may help create content, concepts and articles. In tandem, you may help to amplify the impact of those articles... through content promotion and link building initiatives. You will have the opportunity to not only manage production of cutting-edge content, but you will also learn to report on the performance of your articles to determine the impact of your work. You maintain a high bar of excellence for each piece of content that gets your stamp of approval. You?ll become an expert in digital and SEO content, staying on the cutting edge of best practices. Responsibilities: Ensure we have a strong understanding...
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Alnylam Pharmaceuticals - Cambridge, MA - The Associate Director, Clinical Pharmacology Writing will be responsible for writing clinical pharmacology and pharmacometric reports and corresponding content in clinical documents, regulatory documents and manuscripts. This position will have direct report responsibilities, supervising junior writers and the work of contract writers on a deliverable. The position reports to the Senior Vice President, Clinical Pharmacology and Pharmacometrics. Responsibilities: Produce high-quality... and on-time clinical pharmacology and pharmacometric documents Independently plan, coordinate, develop, update, and revise key documents pertaining to clinical pharmacology and pharmacometrics, including pharmacokinetic reports, pharmacodynamic reports, QTc reports, modeling reports, white papers, and related documents. Other writing activities include clinical pharmacology contributions to clinical documents (eg, investigatorâ??s brochures and clinical study reports), health authority briefing books...
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Valnet Freelance - Nashville, TN - ! We are looking for a Freelance Features Writer who is able to contribute daily to our site. If youâ??re the right fit for our growing editorial team, please apply today! Only serious candidates with strong knowledge of the automotive world will be considered. Job Responsibilities: A minimum of 5 features per week (800 words) Monthly Bonuses Work under tight deadlines and submitting tasks on time Report to Lead Editor and implementing feedback efficiently Application Requirements: C.V. and Cover Letter Links... to published work appreciated, though not necessary Skills Required: Excellent research skills - we do not accept plagiarism of any kind. Broad knowledge of car history and culture. Relevant experience in writing and editing. A solid grasp of the English language and the ability to communicate niche ideas to a wide audience We will get back to you as soon as possible if we think you'd make a solid addition to the team. If you are committed to generating articles with high audience engagement...
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East Harlem Tutorial Program - Harlem, Manhattan, NY - Positions Report to: Manager, College Success Curriculum Development Start Date: June 1, 2021 Professional Development Sessions: June 28th - July1st Program Start Date: July 6, 2021 End Date: August 2, 2021 Hours: Virtual classroom time on Tuesdays and Thursdays 10:00am - 1:00pm; plus 4 hours per week of writing conference time with students and 5 hours per week of prep time, flexible scheduled Who We Are EHTP began in 1958 as a children's reading group and has since grown..., and coaching; to embrace and advance our use of technology; to deepen our embodiment of ethical and equitable radical humanity; and to efficiently operationalize teaching, learning, community, and care. For more information about East Harlem Tutorial Program, please visit us at . About the Opportunity As the Summer College Writing Instructor for EHTP's College Success Institute you are responsible for designing and instructing the â??Introduction to College Writingâ?, an intensive writing course for 25...
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Lexicon Genetics Incorporated - The Woodlands, TX - Lexicon Pharmaceuticals is currently recruiting for an agile, results focused Senior Manager/Associate Director, Medical Writing. This role can be based remotely or in our Woodlands, TX or Basking Ridge, NJ locations. Job Summary: The Senior Manager/Associate Director, Medical Writing will report to our Vice President, Clinical Operations and will focus on writing, reviewing and editing clinical protocols, amendments to protocols and clinical study reports (CSRs). This role will serve... as a lead in generating meeting materials (presentations and posters) , drafting abstracts and manuscripts of clinical study results and providing input into corporate press releases. Key Responsibilities include, but will not be limited to: Providing medical writing support for clinical protocols, statistical analysis plans (SAPs), CSRs and high-level summary documents included in regulatory submissions in accordance with ICH guidelines and established style guidelines. Manages review process in...
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Princeton, NJ - Reporting to the Information Services FInancial-Administrative Systems Administrator in IT, the Technical Analyst/Report Writer is responsible for the creation, documentation, and support of hospital wide core/standardized reports from the hospital's reporting databases (Meditech) and other databases. The report writer will also provide end-user training on report writing software and develop/support users in ad-hoc report creation as needed. Works with Information Services Financial-Admin... data mining techniques across the PCH enterprises in order to provide knowledge to enhance our business processes and improve quality. Qualifications REQUIRED: Formal Education & Certifications: Requires a bachelorâ??s degree in Computer Science or related field Knowledge and Experience: At least one year of programming and/or report generation with report writing tools such as Access, Business Objects, Crystal Reports, etc. Experience with web-based databases and scripting desirable...
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Criterion Edge - San Luis Obispo, CA - of regulatory-compliant Clinical Evaluation Report (CER) projects with top industry clients. Criterion Edge (CE) is seeking a remote candidate for the role of Director, CER Writing Services. The position is responsible to provide management oversight and regulatory/scientific writing expertise to support and lead multiple CER writing projects that support EU MDR regulatory submission requirements for the clientâ??s portfolio of medical device products. Please note that previous CER writing experience...Job Type: Full-Time, Remote Experience Level: Experienced At Criterion Edge, weâ??re committed to empowering companies to deliver better healthcare solutions. By leveraging best-in-class writing processes, technology, and expertise, we empower healthcare companies to achieve their global regulatory goals with superior quality, speed, and budget control. Be on the leading edge by applying your regulatory writing expertise and leadership skills to the development, management and writing...
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YSS - Iowa - The SQL Report Writing Intern will collaborate with the QA Manager and program staff to gather requirements, develop, and manipulate reports by translating data from the client management system into meaningful reports. Job Duties: Attend training related to report writing and analytics within the YSS client management system Create queries to obtain information needed on reports Format data into a usable report for staff to use Assist in building custom forms in the CMS All other duties...
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