Freelance Article Writers : Columbia, Missouri

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Lauren Elliott - Freelance Writing & Article Writing
1
Kudos
5.0
2 Skills
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Rate/Hr
I am a published travel writer. I have helped with writing, proofreading and editing hundreds of journal articles for physicians in the Columbia, Missouri area, and have assisted in the preparation/typing, proofreading and editing of 3 books. In addition, I was a photojournalist in the U.S. Marine Corps; in this position, I wrote squadron newsletters and articles for publication. My career...
Columbia, Missouri, United States
Caitlin Coyne - Freelance Article Writing & Biography Writing
0
Kudos
3.0
2 Skills
$15
Rate/Hr
Caitlin Coyne 205 S. Garth Avenue Columbia, MO 65203 573-303-1636 catcoyneagency@gmail.com www.about.me/cat.coyne Work Experience Editorial Assistant, Professional Editing Services LLC Columbia, Missouri, May 2012—Present • Assisted the head editor by proofreading, editing, researching, and writing articles, business plans, biographies, and various other projects as assigned...
Columbia, Missouri, United States
Gina Stewart - Freelance Article Writing & Writing
0
Kudos
4.5
2 Skills
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Rate/Hr
Work Experience Jan. 07 – Present Freelance writer, SEO writer * Various online companies and individuals Aug. 05 – Feb. 07 Columbia Business Times (Newspaper) Freelance Reporter * Covering meetings, features and anything newsworthy * Familiar with AP Style * Relaxed interviewing style that got many people talking when they were afraid or didn’t want to Jul....
Columbia, Missouri, United States
Tyler Garnes - Freelance Article Writing & Writing
0
Kudos
3.0
2 Skills
$10
Rate/Hr
I've been pursuing a writing career for some time now and am more skilled in advice writing. I have also done a bit of article writing before that and fiction writing specialty short stories.
Columbia, Missouri, United States
Alex Denison - Freelance News Photography & Article Writing
0
Kudos
4.5
2 Skills
Ask
Rate/Hr
Writer for hire.
Columbia, Missouri, United States

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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
Hilda Boeringa - Freelance Photography & Outdoor Photography
1
Kudos
3.0
2 Skills
Ask
Rate/Hr
Professional Profile Dependable, muti-task-oriented and energetic with exceptional interpersonal and decision-making skills. Strong work ethic, professional demeanour and great confidentiality qualities. Core Qualifications * Photography, outdoor/indoor • Executive management support • Excels in scheduling • Proficient computer skills • Strong leadership skills • Critical thinker, self-starter with professional manner • Energetic, organized with superior attention to detail • Effective time management and prioritizing • Team player and works very well independently • Strong verbal and written communication skills • Excel in client/patient relations • Extensive experience in data collection and data entry Career Accomplishments Photography * Sports photography for volleyball team, soccer, hockey * Event photography for Stephanie McIlroy, singer/songwriter. * Published photos in newspapers and event issues Scheduling • Coordinated daily schedule for principal and various board meetings with affiliate committees. • Conference bookings with principal and faculty, interview scheduling for various positions. • Corresponded with patients through phone, fax, email, and in person to schedule appointments. • Day-to-day scheduling for medical doctor outside of medical office. • Travel planning for domestic and international destinations, ensured concise itinerary information. Operations • Accountable for all operations of busy medical office, including all patient inquiries, telephone calls, scheduling appointments, referrals to specialists, billing, charting, filing, routing laboratory results, and medical transcription of patient records. • Screening calls for principal, medical doctor and staff. • Regular inventory and ordering medical/office supplies. • Regular updates to medical doctor’s Curriculum Vitae as accomplishments, experience, staffing appointments and hospital titles were achieved. Training, Supervising and Leadership • Responsible for training and supervising all temporary staff, medical secretary students, volunteers and part-time/casual help to ensure continued quality of patient care and smooth office operations. • Leadership within Education Board, Hiring Committees, classroom visitations, principal evaluations and collaborating Education / School Policies for implementation. • Staff selection interview leadership. Data and Office Organization • Improved office organization by compiling running schedules and agendas. • Reorganized medical filing system to ensure proper accessibility for staff and physician. • Ensured necessary patient information packages and technical library information were printed and /or ordered for continued distribution. Meeting / Event Preparation and Administration • Prepared agendas and minute-taking for Education Board, School Board and various committees. • Coordinated meetings, events, programs and commemorative book. • Coordinated food services, keynote speakers, guest speakers, and international physician, travel, and accommodation arrangements for various events. Employment History July 2011 to Executive Administrative Assistant October 2011 Human Resources Dept., Community Care Access ~London, ON February 2011 to Executive Administrative Assistant to the Prinicipal March 2011 Kings University College, UWO ~London, ON Temporary contract February 2001 to Medical / Executive Assistant June 2010 Allergy, Asthma and Immunology, Dr. A. Belda ~London, ON Full time February 1992 to Secretary / Receptionist July 1993 Extendicare London ~London, ON Full time April 1999 to Secretary July 1993 Standard Life (Group Pension Administration) ~London, ON Temporary contract Certifications/Diplomas • Accident and Sickness Disability Insurance (2012) Provincial Licensing • WHMIS Training Certificate (2008) * Lambton College Photography Course (2007) • Medical Clerk Certificate (2007) Honours Lambton College ~Sarnia, ON Medical Terminology, Medical Office Procedures, Working and Communicating in a Medical Setting, Microsoft Word Specialist, Microsoft Excel Specialist, Medical Conditions for the Medical Office Professionals, Understanding Surgical Procedures for the Medical Staff • Word Processing Certificate (1992) Honours Westervelt Business College ~London, ON Business Language Fundamentals, Computers, Lotus 123, WordPerfect, Typing, Office
Toronto, Ontario, Canada
Deborah Badmus - Freelance Paralegal & Blog Writing
0
Kudos
3.0
2 Skills
$20
Rate/Hr
RESUME OBJECTIVE: LAW CLERK/ LEGAL ADMINISTRATIVE ASSISTANT HIGHLIGHTS • Problem-solving; analytical and research-oriented • Several years in legal and administrative environment • Advanced skills with Microsoft Word, Outlook and PowerPoint • Advanced communication, drafting, collation and writing skills • Technical knowledge in contract preparation and negotiation • Adept use of QuickLaw, WestLaw and CanLII research tools • A team player; interfacing effectively at all organizational levels • Ability to manage high volume clientele in a demanding environment • Able to work independently; results-oriented and positive professional EDUCATION 2014 Entrepreneurial Program (Training & Business Plan) Ministry of Training, Colleges & Universities, Graduation Certificate 2010-2011 Accreditation, National Committee on Accreditation University of Toronto Law School, Certificate of Qualification 2007-2008 Co-op Program/Microsoft Office Yorkdale Adult Learning Centre, North York, Toronto Certificate for credits received 2005-2006 Corporate Law Clerk Program Legal and Corporate Administration- Graduate Certificate Seneca College of Applied Arts & Technology, Toronto RELATED LEGAL WORK EXPERIENCE 2014 Independent Law Clerk (Present) DEB BUSINESS SERVICES (Legal, Corporate & Admin.) • In-depth Market Research involving Primary/ Secondary Research and Analysis • In-depth research of relevant Legislation and case-law to determine applicable Law • Design of Business Cards, Flyers, Letterhead, Email Signature and Complete Website • Thorough Collation, Compilation & Drafting of Business Plan & Executive Summary • Development of Networking, Sales, Market and Business Implementation Strategies 2012-2013 Articling Student-Personal Injury Law (6 Months) GALAN LAW FIRM Barristers & Solicitors • Perusal and maintenance of Personal Injury electronic and paper files • Attendance at Mediation and Court for Civil Matters and Criminal Trials • In-depth research of relevant legislation and case-law using legal soft-ware • Drafting of Factums, Statements of Claim/ Defence and Notices of Appeal • Drafting of Motions, including Consolidation and Substituted service motions • Preparation of Motion Records and binders for service on parties to Actions • Contact with Defence Counsel/ clients for clarity of clients position • Court house searches (on-line & file room) for document discovery • Preparation for and questioning at Examinations for Discovery 2007 Real Estate Law Clerk (Co-op) AARON & AARON, Toronto Barristers & Solicitors • Obtained discharge of charge particulars and documents • Made production requests to vendors’/purchasers’ Lawyers • Forwarded discharge particulars in fulfilment of Undertakings • Contacted Vendors’ Lawyers for fulfillment of their Undertakings • Filled out general and trust account bank books for payment • Deposited cheques/ mortgage funds into appropriate accounts • Drafted correspondence and filed documents; other admin duties • Reception duties; took calls and re-directed them as appropriate • Perused files for discovery of outstanding issues for closure 2006 Defense Litigation Law Clerk (Contract) REISLERFRANKLIN LLP, Toronto Barristers & Solicitors • Briefed incoming documents on an ongoing basis • Produced documents requested by opposing counsel • Used Amicus Attorney software for billing, searches, appointments • Organized trial, arbitration and medical briefs in preparation for trial • Prepared reports, undertakings, affidavits of documents and summaries • Reviewed productions and discovery transcripts • Reviewed reports of mediators and updated briefing • Handled telephone inquiries from clients and counsel • Prepared authorizations for release of information • Prepared documents for examinations for discovery • Prepared disclosures, legal documents and reports OTHER RELEVANT LEGAL EXPERIENCE OVER 10 YEARS
Bowmanville, Ontario, Canada
Tiandra Callaway - Freelance Creative Writing & Poem Writing
1
Kudos
4.0
2 Skills
Ask
Rate/Hr
Tiandra M. Callaway 2624 Scott St. Apt. B Little Rock, AR 72206 Phone: 859 433 0124 E-mail: tmc279@hotmail.com Summary of Qualifications *Thirteen (14)+ years of writing experience, established through personal interest *Literature and journalism influence while acquiring B.A. degree *Five (6)+ years of proofreading for peer development Summary of Publications *Multiple www.poetry.com submissions under my name, no pseudonyms *Nature’s Echoes anthology submission, 2002 *Various articles for the Kentucky State University newspaper, The Thoroughbred News, 2002-2003 *Kentucky State University’s annual literary magazine, The Kentucky River, 2004 Work Experience *Faculty, Arkansas Baptist College, Little Rock, AR - current *Former teacher of English for Fayette County Public Schools, Lexington, KY *Organizer of 7th grade portfolios at Scott County Middle School for CATS, Kentucky *Proofreader for a University of Kentucky doctorate student in Educational Administration *Administrative Assistant II for the Kentucky State University Department of Social Work and Criminal Justice where dictation, proofreading, and typing were a few duties given to perform by the immediate supervisor *Co-editor of Kentucky State University’s literary magazine, The Kentucky River *Teacher’s aide and student teacher positions for classroom experience Writing Skills *Ability to write multiple pages of original, cohesive, and genre-specific material *Ability to create, artistically and technically, many forms of poetry, prose, articles, speeches, agendas, proposals, etc. *Ability to proofread multiple pages of familiar and unfamiliar texts *Ability to meet deadlines when dealing with any number of pages and topics *Apprentice skills in copyediting, gaining knowledge Education Bachelor of Arts, English with literature concentration, 2004 GPA: 3.52/4.0 – Magna *** Laude graduate, Departmental Honors Kentucky State University, Frankfort Master of Arts, Education with Secondary English concentration, 2007 GPA: 3.91/4.0 – Summa *** Laude graduate University of Kentucky, Lexington Activities/Interests *Community service for various organizations including, but not limited to, the Sickle-Cell Anemia Foundation, Big Brothers/Big Sisters, and the March of Dimes *Participation in youth development and care, especially concerning media influence *Development of writing techniques and maturity *Host and participant in several open-microphone poetry sessions *In the process of writing three (3) books: a children’s book, fiction, a tribute to fathers *Writer of poetry and short stories *Music, comedy, and media studies
Little Rock, Arkansas, United States
Cassandra Carrascosa - Freelance Photo Editing & Photography
0
Kudos
5.0
2 Skills
$25
Rate/Hr
I'm a photography college student seeking free-lance work in photo editing and retouching. My editing skills are at a professional level due to my artistic background. My expertise being in fine art photography, and I’m passionate about creating anything in the abstract. Most of my work consists of combining multiple exposures, while I also work with influential music theory, and symbolism. I continually strive to experiment with new processes and ideas. For instance, a direction I am gearing towards focusing on in the very near future is mixing mediums. (i.e. printing on alternative surfaces, and digital image transfer) I will be graduating with my Associates of Fine Arts in December 2013. o Skilled in Photoshop, Lightroom, and Microsoft Word o Adept in After Effects CS6, and Premier o Advanced Image Retouching and manipulation o Intermediate Graphic Design o Self starter, motivated, passionate
Hutchinson, Minnesota, United States