Freelance Article Writers : East Ayrshire

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Jason Thorne - Freelance 3D Animation & 3D Graphic Design
0
Kudos
4.5
2 Skills
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Rate/Hr
Free lance motion graphic / VFX artist. i've studied a BA degree in motion picture, and have extensive experience in several post production software packages, aswel as 3D. i use Maya predominately , along with VRay.
South Africa
Lawrence Sanata - Freelance Content Writing & Creative Writing
0
Kudos
5.0
2 Skills
$40
Rate/Hr
Lawrence Sanata 5216 Dublin Road Delaware, OH 43015 740-816-0766 lsanata@yahoo.com Objective: Infectiously enthusiastic and highly experienced professional seeks challenging, fast-paced and full-time corporate communications, marketing communications or public relations position. • Highly accomplished with a track record of creating strategically impactful internal and external communications, including web content • Extensive background in organizational communications and crisis communications, as well as B2B and B2C messaging • Recognized for superior writing skills and highly refined organizational skills in creating persuasive and powerful communications ______________________________________________________________________________ Professional Experience: Editor Classic MG Columbus, OH November 2013-Present • Create compelling and entertaining stories about MG automobiles and their owners for this nationally circulated car magazine • Promote this specialty publication’s vision as the leading source of information in the U.S. about classic MG automobiles • Help to establish editorial calendars and oversee contributing writers and photographers Owner Red Splash Studio Columbus, OH June 2012-Present • Craft innovative and strategic internal and external communications, as well as marketing collateral, for clients of all sorts and sizes • Develop creative web content, with an emphasis on powerful testimonials and persuasive storytelling • Prepare compelling press releases that generate brand interest and loyalty Director of Public Relations Adena Health System Chillicothe, OH October 2009-June 2012 • Launched a highly successful media campaign using compelling press releases and op-ed pieces that successfully portrayed the health system and its physicians and staff • Created highly successful and engaging internal and external newsletters for employees as well as a quarterly magazine distributed in the communities served by Adena • Partnered with senior executives in developing successful communications strategies and tactics for an assortment of projects • Compensated through Writing Assistance Inc., which had a contract with Adena Marketing Communications/Brand Voice Writer JPMorgan Chase Columbus, OH: June 2007-June 2009 • Created new and compelling brand language and messaging to more effectively communicate with clients and wealth advisers • Developed strategic marketing collateral and change communications that resonated with clients and prospects Corporate Communications Consultant Columbus, OH August 2006-June 2007 • Created persuasive web content for Access Credit Lines, Cogent Search and Dublin Metro Dental in Columbus, OH and Integrated Printing Solutions in Denver, CO • Developed branded B2B and B2C messaging for EmergiTech in Columbus, OH and Integrated Printing Solutions Medical Marketing Communications/Brand Voice Writer inChord Communications Westerville, OH November 2004-July 2006 • Developed successful brand-targeted marketing materials, including brochures and sales aids, and provided editorial direction for global pharmaceutical clients, including Bausch & Lomb, Eli Lilly and Genentech • Partnered with senior management and creative team members to carry through imaginative strategies and tactics Marketing/Public Relations Consultant and Freelance Writer Sharpsville, PA October 2002-November 2004 • Generated persuasive marketing and public relations communications for a variety of clients, including medical and technology businesses, and a Pennsylvania college • Crafted entertaining news and feature stories for print and online magazines, including AMC Outdoors, AutoWeek, Building Online Business, Classic Motorsports, Columbus CEO, DreamGarage.com and Roundel Medical Writer/Government Writer Pittsburgh Tribune Review, Pittsburgh, PA July 1999-October 2002 • Created powerful news and feature stories about public health and medicine, and helped to launch this newspaper’s first anchored health section • Developed issues-related government and political stories while developing a presence for this newspaper in the fastest-growing county in western Pennsylvania Academic Background: • Youngstown State University, Youngstown, OH, Bachelor’s degree in English/Journalism
Dublin, Ohio, United States
Archana Gupta - Freelance Editing & Proofreading
0
Kudos
5.0
2 Skills
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Rate/Hr
ARCHANA GUPTA lEmail: mahajanarchana30@gmail.com l Phone: (647) 427 4039 OBJECTIVE I am a keen learner and enjoy the challenge of leading initiatives and consistently delivering results. I enjoy working with and learning from a diverse group of people. ACADEMIC QUALIFICATION Post Graduate Diploma in Mass Communication, Panjab University, India 2005 – 2006 Post Graduation in English, Panjab University, India 2003 - 2005 WORK EXPERIENCE Assistant Production Editor PEARSON EDUCATION, Chandigarh, India July 2007– September 2009 · Maintained high standards in accuracy, adhered to quality checks at each stage of pre press · Prepared reports, maintained schedules and ensured timely processing of vendor bills · Met publishing deadlines, organized copyediting, typesetting, proofreading and project management Freelance Editor/Proof reader PEARSON EDUCATION, India January 2007 – July 2007 · Edited and proofread work from the manuscript stage to the final stage of pre press. Research Assistant THORPES EDUCATION, Chandigarh, India January 2007 – July 2007 · Worked in assistance with the author for new content and updating the works. Edited and proofread the works. Management Trainee ERCO TRAVELS, New Delhi, India April 2003 – July 2003 · Had the opportunity to learn and have an insight into the working of various departments of the company and an overall view of the travel trade. SKILLS · Microsoft Word · Adobe Acrobat INTERNSHIPS CII, Chandigarh, India November 2002 · Worked with CII in Textech 2002 held at Chandigarh HDFC Standard life Insurance, Chandigarh, India October 2002 · Worked with HDFC Insurance in Consumer Fair 2002 held at Chandigarh EXTRACURRICULAR ACTIVITIES · Organized Film Festival for M.C.M. college as a member of film-club SANWAD (26–29 October, 2005) · Prepared Photo Profile for M.C.M. College · Prepared photo feature on the Beautiful and the Ugly side of the City Chandigarh · Research work on The Man Who Speaks Through His Lens-Raghu Rai LANGUAGES KNOWN English, Hindi
Toronto, Ontario, Canada
Steph Pickard - Freelance Fashion Photography & Magazine Photography
5
Kudos
3.5
2 Skills
$100
Rate/Hr
Hey! I'm Steph, I'm a 22 year old photographer based out of Metro Detroit. I've worked as a photographer throughout high school and college working for PR companies, fashion magazines, as a staff photographer for MSU's yearbook, as well as other companies and organizations. I graduated with a Bachelor's degree in photography this past May, and since then have worked at two different studios studying under two very talented photographers. Now, I'm pursuing my career as a photographer with a strong interest in editorial and lifestyle portraiture. I hope to accomplish a flourishing career in lifestyle fashion photography and one day relocate from Detroit to the Rocky Mountains. I'm extremely motivated, outgoing, independent, and a very confident self-starter. Outside of photography I love traveling, camping, snowboarding, and jamming out to classic 70's-80's rock music.
Detroit, Michigan, United States
Reinaldo Fernandez - Freelance Spanish Translation & Italian Translation
0
Kudos
4.5
2 Skills
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Rate/Hr
CURRICULUM VITAE PERSONAL DATA NAME : Reinaldo José Fernandez Blohm BIRTH PLACE AND DATE: Caracas, 17 de Junio de 1967 STATUS: Single ADDRESS AND PHONE: La Boyera, calle B, Res. Los Geranios 24-A, Tlf 6352436 / 0412 8044555 EDUCATION UNIVERSITY OF DUBLIN, CALIFORNIA: B. A. Communications SECCIONAL APOYO DOCENTE LOS TEQUES: High School Diploma AMADEUS VENEZUELA: Basic and Intermediate Amadeus Global Reservation System AEROTRAFFIC: Basic Air Traffic and Reservations course IETASA: Tour Package design LANGUAGES Spanish, English, Italian WORK EXPERIENCE (2010) Wall Street Institute: Service Manager/Teacher (2005 / 2006) Cacao Travel Group: Tour Operator (2004 / 2005) LIBRERIAS LAS NOVEDADES: Manager, Hotel Tamanaco bookstore (2002 / 2004) I.P.S.F.A. : Protocol Assistant, Public Relations Department (2001/ 2002) IFAMIL VIAJES Y TURISMO: Travel Agent (1998 / 2001) BODEGON VISTAMAR PUERTO LA CRUZ: Manager, Liquor store
Barquisimeto, Lara, Venezuela
Dallas Thomas - Freelance Quality Assurance & Consulting
0
Kudos
3.0
2 Skills
$90
Rate/Hr
Dallas L. Thomas, RAC, MHA, MPA, SSYB, Certified Lead Auditor West Palm Beach Area, Florida, USA Mobile/Work Phone +1 801 613 2601 Email: thomas.regulatory@gmail.com Global Regulatory Affairs & Quality/Compliance/Auditing PROFESSIONAL PROFILE: A focused, driven, and passionate regulatory affairs and quality/compliance/auditing professional with hands-on experience in RA and Quality/Compliance/Auditing associated with activities which lead to, and maintain regulatory approval to ISO 13485, FDA 510(k), EU CE Mark & other international market authorizations of medical device products and conformance/compliance of Quality Management Systems. Regulatory Affairs Certification (RAC). Certified Lead Auditor for ISO 13485. Certified Six Sigma Yellow Belt. Experience working with multi-disciplinary teams. Proven organization and time management skills with ability to multi-task under stress. Exposure to national & international regulatory standards such as GMPs, ISO 13485, ISO 9001, QSRs, 21 CFR part 820, Food Drug and Cosmetics Act, RDC 185, and MDD 93/42/EEC, among others. Ability to work well under pressure and handle multiple projects and meet multiple deadlines, while managing priorities accordingly. Prior team building/management and supervisory experience. 2 master’s degrees (Health Administration & Public Administration). Fluent in Spanish and Portuguese. Experience: Chemular (subsequently via Hudson Scientific), Michigan - Quality and Regulatory Consultant (July 2016-Present) ? On Site Quality Management Systems auditing, as lead auditor. ? First time implementation of a QMS ? Prepared client companies for ISO Certification Audits ? Assess for Non-Conformities of Quality Management Systems requirements and propose corrective and preventive actions for compliance. ? Client Training on Management Review, External Audit Preparation, All Employee Training on Quality Management Systems ? Technical File Preparation Axiom Medical, California- Remote Member of UDI Support Team (September 2016) via consulting firm partner company ? Unique Device Identification (UDI) associate consultant ? Assist with Gathering and Uploading data to FDA GUDID before deadline US Ophthalmic, Miami, FL - Quality and Regulatory Consultant (June 2016-Present) ? Unique Device Identification (UDI) general guidance to client ? Quality Management Systems preparation for 13485 Certification ? First time implementation of a QMS ? Revision to QMS for preparation of 13485 Certification Face View Mask, Inc., Virginia - Remote Regulatory Affairs Consultant (December 2015-January 2016) via consulting firm partner company ? Premarket Regulatory Assessments ? Label reviews for conformance to US and EU markets ? New Technical File and first time CE Mark for Radiographic Ophthalmology Device ? Review of Applicable Guidance Documents ? Classification of Devices for FDA submission pathway and using rules from MDD 93/42/EEC Acuderm Inc., Fort Lauderdale, FL- Regulatory Affairs Consultant (March 2016-Present) via consulting firm partner company ? Project manager for team of 5 for EU Technical File Updates and Remediation and response to Notified Body major non-conformities, minor non-conformities and observations. ? Remediating various Tech File deficiencies from notified body audit including Risk Management, Essential Requirements Checklist, Post Market Surveillance, and Labeling ? Coordinated remediation of deficiencies with SMEs in Verification and Validation, Design Controls, Clinical Evaluation Zimmer Biomet, Palm Beach Gardens, FL- Senior Regulatory Affairs Specialist (January 2016 –Present) ? Preparation and member of ANVISA (Brazilian Agency) GMP Audit Team ? Certified Lead Internal Auditor for ISO 13485 Scope and Internal audits of Quality System ? New Product Development Regulatory Representative responsible for regulatory pathway assessments for FDA 510(k), Letters to File, EU CE Mark Technical Files, Health Canada new applications and amendments. ? Participate as representative in the change control process for proposed changes to product design, supplier and raw material changes, labeling changes. ? Notification of changes to Global counterparts for regulatory impact assessment of changes in all geographies and providing ? Regulatory affairs projects and submissions for class I and II US FDA 510(k) support and Letters to File, Health Canada Submissions (Class I, II, III, and IV) CE Mark (Class I, II and III) and notified body communications. ? EU Technical File Updates and Maintenance and preparation for notified body audit. ? Internal Auditor of the Quality Management Systems per 21 CFR 820 and associated regulations and auditing of multiple internal departments. ? Participated as company audit scribe and crucial audit team member in multiple external audits (Notified Body, Microbiology, FDA prep) ? Regulatory Affairs Database creation of records and maintenance in Oracle, Discoverer, and Application Express Interface ? Creator of online web interface tracker for global regulatory project and task requests from global and internal contacts for internal prioritization. ? Continued support of Latin America geographies as needed. Zimmer Biomet (after merger), Palm Beach Gardens, FL- Senior International Regulatory Affairs Specialist (January 2015 –January 2016) ? Moved from consultant to employee and continued work on items below, along with additional depth and responsibility in those areas. Biomet, Palm Beach Gardens, FL- Regulatory Affairs Consultant (July 2014 –January 2015) ? Device Registrations and Device Renewals and tracking in Latin America geographies. ? Internal training to applicable SOPs, protocols, and procedures. ? Assist with Product Change Notifications to global geographies as needed. ? Fixing multiple registration errors done by Ministries of Health and prior internal employee generations. ? Set up registration records of current product registrations for future reference and organization. ? Obtained dozens of first time registrations and dozens of renewals/product sustaining work across the entire Latin America geography and a variety of MOH’s. ? Interfacing with regulatory contacts within company subsidiaries and third party contract distributors in Portuguese and Spanish on a daily basis in both written and spoken formats. ? Researched and translated native-language Latin America regulations to implement a compliant regulatory strategy in harmony with COFEPRIS (MX), ANVISA (BR), DNM (El Salvador), INVIMA (Colombia), DIGEMID (Peru), and ANMAT (Argentina) among others. ? Due diligence to in-country standards and regulations for labeling, pre-market authorization and clearance as well as post-market compliance to in-country requirements. C.R. Bard, Inc., Bard Access Systems Division, Salt Lake City, UT-International Regulatory Affairs Specialist (October 2013 –July 2014) ? Obtained RAC-Certification (EU) for the scope of all regulated sectors (Pharmaceuticals, Medical Devices, IVDs, etc.) after proven self-study and examination of the Regulatory Affairs Professionals Society (RAPS). ? Successfully drove, coordinated, and completed multiple International Dossier Submissions for First Time Registrations of various product families in the markets of Asia, Latin America, EEMEA, and other core geographies. ? Successfully CE-Marked many products according to the Medical Devices Directive 93/42/EEC including direct responsibility for the Essential Requirements Matrix and the Declaration of Conformity. ? Participated in relevant phases of design control activities as needed. ? Maintained updates to CE technical files for compliance purposes. ? Notified global regulatory counterparts on changes to product design, IFUs, labels, sterilization, etc. ? Maintained direct contact with company representatives around the globe in Asia, Latin America, EEMEA, Europe and Australia. ? RA Representative and Portuguese Translator for Brazil Deep Dive Team in Sao Paulo and Curitiba, Brazil ? Portuguese Translator for Brazilian Nurses at Infusion Nurses Society (INS) Event 2014 in Phoenix, AZ. C.R. Bard, Inc., Bard Access Systems Division, Salt Lake City, UT-International Regulatory Affairs Associate (January 2012 – September 2013) ? Trained and acted in Capacity of Internal Auditor including training to 21 CFR 820, FDA Quality System Regulations, and ISO 13485. Revised department procedures. Participated in label audits and audits of other departments as called upon by Lead Auditors. ? Successfully drove and completed multiple International Dossier Submissions for First Time Registrations of various product families in the markets of Asia, Latin America, EEMEA, and other core geographies. ? Successfully CE-Marked products according to the Medical Devices Directive 93/42/EEC including the Essential Requirements Matrix and the sign off of CE Declaration of Conformity by management. ? Dozens of international regulatory submissions and a signatory to reformatting/updating/maintaining EU Technical Files and Design Dossiers including, DOC, ERC, and compilation of additional appendices of supporting documents in areas of QMS, Risk Management, Sterilization, Biocompatibility, Design Verification and Validation, Shelf Life, Labeling, etc. in remediation and preparation for a notified body audits. Utilized GHTF (now IMDRF), Team NB Med, and MDD 93/42EEC guidance documents and templates to feed internal formatting and SOPs. ? Participated in relevant phases of design control activities as needed. ? Maintained updates to CE technical files for compliance purposes. ? Notified global regulatory counterparts on changes to product design, IFUs, labels, sterilization, etc. ? Maintained direct contact with company representatives around the globe in Asia, Latin America, EEMEA, and Australia. ? Efficiently assessed product modifications and updates to labeling and IFUs in order to maintain regulatory compliance and approve allowed changes. ? Worked directly with our Portuguese and Spanish speaking counterparts in Brazil and Mexico in order to ensure efficient and productive product submissions, renewals, and sustaining of currently registered products. Lead conference calls with Latin America Regulatory contacts in Portuguese and Spanish. ? Worked directly with multi-disciplinary teams in order to provide regulatory assessment on product modifications, upgrades, label changes, IFU modifications, etc. ? Interfaced directly with cross-functional departments in order to acquire relevant regulatory information from R&D, Quality, Biocompatibility, and Sterilization Departments in order to supply to company business centers worldwide. ? Trained all immediate team members on International Product Submission Dossiers per appropriate corporate and division-level protocol, as I was a founding member of the International RA team. ? Responded to registration deficiencies from ANVISA (Brazil), COFEPRIS (Mexico), CFDA (China), MHLW (Japan), and various competent authorities in Europe. ? Supported hospital tender/contract requests for regulatory information globally. ? Received, prioritized, and concluded hundreds of International Regulatory requests related to implantable port-catheter products such as document requests, hospital tenders, and additional registration activities. ? Supervised and trained two intern staff members who reported directly to me for their projects and workload. ? Participant on corporate-wide committee to update the corporate international dossier protocol. C.R. Bard, Inc., Bard Access Systems Division, Salt Lake City, UT-Domestic U.S. Regulatory Affairs Intern (April 2011 – December 2011) ? Regulatory representative on US domestic team for Implantable Ports and Catheters for both power-injectable and non-power injectable ports, port kit components and accessories, as well as assisting with regulatory device labeling and packaging requirements for Corporate-level, FDA 510(k) submission support, and compliance to the Food Drug and Cosmetics Act, and 21 CFR 820. ? Regulatory support for both new product development (NPD) and sustaining existing products with their respective modifications (notes to file/notification of change). ? Assisting in determination of the appropriate regulatory submission requirements and strategies for new or modified products. Prepared required documentation as needed. ? Supporting coordination and review of FDA submissions and test protocols with Corporate Regulatory, Medical and Legal Departments, and respond to any questions posed by these departments or the FDA. ? Confirming translations of international regulatory/labeling/marketing documents in the Portuguese and Spanish languages prior to submission. ? Supporting the review of proposals for new product development as well as modification of current medical devices in order to meet regulatory submissions. ? Representing regulatory affairs on product development teams to provide assistance with respect to regulatory requirements and strategy. ? Assisting in development of new product instructions for use/promotional and advertising material including labels and labeling. Reviewing product labeling for compliance with medical device regulations and Division/Corporate Policies. ? Providing marketed product regulatory support for change management activities, product registrations, and business improvement activities. ? Drafting and submitting notifications of change to notified bodies/authorized representatives for international regulatory submissions to BSI, Medicon, and corporate-level international business centers. Compiling support documentation for said notifications of change. ? Verified and updated hundreds of data points for product-line specific regulatory database in order to maintain current and accurate regulatory data from the past and present. ? Acting as support in tracking engineering change notices (modifications to products) in order to verify appropriate regulatory implications in relevant domestic and international markets. Deseret Industries, West Valley City, UT- Department Manager/Job Coach Trainer (June 2008 – Jan 2012) ? Supervised up to 21 associates concurrently, across 3 departments to reach production and sales goals. ? Coordinated and collaborated on associate hours budgeting to reach Total Budgeted Operations goals. ? Ensured quality standards and policy alignment in production areas. ? Resolved customer issues and concerns and provided 100% customer satisfaction. ? Completed several key company goals regarding new pilot program implementation. ? Utilized MS Office Suite for company operations, forms, schedules, tracking goals, and evaluating product sales. EDUCATION: University of Utah-Salt Lake City, UT ? Masters of Health Administration, David Eccles School of Business, 2010-2013 (Emphasis in device regulatory affairs) ? Masters of Public Administration, Center For Public Policy and Administration, 2010-2013 (Emphasis in device regulatory affairs) Brigham Young University-Provo, UT ? Bachelors of Science in Human Development, 2005-2008 Utah State University-Logan, UT ? General Education Coursework, 2004-2005 (Portuguese Coursework) (Spanish Coursework) ADDITIONAL TRAINING: ? FDA Design Controls, Palm Beach Gardens, FL, 2014 ? BSI Medical Device CE Marking Seminar, San Diego, CA, 2012 ? FDLI Brazil Conference on Medical Device Registration, São Paulo Brazil, 2012 ? Latin America Life Science Regulatory Affairs, New Orleans, LA 2013 ? Crucial Confrontations Leadership Training, Salt Lake City, UT 2014 ? Bard Brazil Deep Dive, RA & Portuguese Translator, 2014, São Paulo & Curitiba, Brazil. ? RAC, Regulatory Affairs Certification—RAPS (Regulatory Affairs Professionals Soc) May 2014 ? ADVAMED 2015, International Committee Member, San Diego, CA October 2015 ? Lead Auditor Certificate (ISO 13485) issued by BSI, Palm Beach Gardens, FL July 2016 ? Internal Auditor Certificate (ISO 13485) issued by BSI, Palm Beach Gardens, FL July 2016 ? ISO 13485 Training Certificate issued by BSI, Palm Beach Gardens, FL July 2016 ? Six Sigma Yellow Belt Certificate issued October 2016 COMPUTER SKILLS: ? PC & Mac literate ? Proficient in Microsoft Office Suite Software (Word, Excel, PowerPoint, Outlook, Access Database) ? PDF Manipulation, editing, and data extraction in Adobe Acrobat ? Additional Software Experience: MFG Pro, Qumas, Docushare, Final Cut Pro, Master Control, SharePoint, Oracle Database, ETQ Reliance, TipQA, InfoPath, Application Express and Oracle Discoverer. LANGUAGES: ? Speaks, reads, writes & translates Professional level Portuguese fluently with on the Job Translation Experience. ? Speaks, reads, writes and translates Spanish with high professional fluency. LIVING ABROAD: ? Lived abroad in Sao Paulo, Brazil for 2 years, establishing Portuguese fluency and leveraging to subsequent Spanish fluency. REFERENCES: Additional References Available Upon Request
Jupiter, Florida, United States
AthenaFawcett - Freelance Public Relations & Photography
0
Kudos
3.0
2 Skills
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Rate/Hr
My name is Athena. I am 25 years old. I am a wife, a mother, a daughter, and a friend. I am a housekeeper for Wyndham Resorts as well as for personal clients. I am also a writer who is in the process of publishing my first book, "Climbing Out of The Darkness", a freelance writer, and a photographer. I have done photography for weddings, engagements, couples, babies, and outdoor photo shoots for families. I am a Jill of all trades. I am an aspiring paralegal studying law at the moment and balancing life. I enjoy writing and photography as they are my hearts desire. I have my own blog space which I would be happy to share at a time of contact. I would also be happy to share any wedding photo samples you may want too look at. I wear many hats. I have worked as a production worker in a factory, a church secretary, a fundraising coordinator, cashier, cook, nursing assistant, volunteer teacher, and housekeeper. My experience in life gives me a great outlook in writing.
Harrison, Arkansas, United States
Janie Abney - Freelance Article Writing & Biography Writing
0
Kudos
4.0
2 Skills
$5
Rate/Hr
My specialty is in article writing and re-writing but have over 2 years experience in a variety of writing and subjects. Writing is my passion and I am a hard worker, responsible, multitasker, computer savvy and lots more. I have done writing for different online companies and have wrote on subjects such as "News, Law, Business, Animals, Natural Disasters, Biographies, Wikipedia re-writes,Family, Science, and many more. I have done Content Writing, Writing for blogs, Research, Re-write content/articles, article writing, and much more. I write to please.
Nicholasville, Kentucky, United States
Oscar - Freelance Drawing & Comic Art
0
Kudos
3.0
2 Skills
$20
Rate/Hr
Hello everyone. Despite the fact that I got some certificates as Multimedia technician and Graphic design, I like much more traditional drawing, subject in which I also got degrees and experience. My main aim is illustrate books, magazines, humour graphic, cartoons, comics... Eventually I'll add more draws in my profile. I hope hearing from you soon. Oscar.
London, United Kingdom
Kevin Klatt - Freelance Editing & Writing
0
Kudos
5.0
2 Skills
$30
Rate/Hr
I've been writing short stories from the age of eleven, when I won my first writing competition. I received a degree in journalism from a small college in Iowa, and my first job after graduation was as editor of a weekly newspaper in northern Minnesota. After that, I was head hunted to become editor-in-chief of a monthly news magazine. But there's a twist. In 1979, while travelling in Ireland, I met the lady who would become my wife. We married in 1980, and in 1981, we moved back to Ireland, where I've resided ever since. The writing bug never left, and in 2004, I wrote and self-published my first crime thriller. I've been doing freelance writing jobs since 2010, and very much enjoy the work. I can supply feedback from those who have hired me, and all I can say is, if you trust me with your writing job, you won't be disappointed. I look forward to hearing from you.
Dublin, Dublin, Ireland