Freelance Brochure Design Jobs : Washington

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21
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San Francisco, CA - Los Alamitos, CA - advocacy organizations and foundations. 2. Manage communications and outreach projects to achieve program deliverables, including those that include external vendors. 3. Write content for a variety of channels and purposes, including: website, social media, emails, press releases, brochure content, and e-newsletter and collateral materials. 4. Coordinate editing, proofing, and/or graphic design work with internal staff and external vendors. 5. Maintain consistency in wording and messaging... across all communications to ensure that CFTL brand is appropriately represented. 6. Participate on work teams to design enhanced web content, including better ways for people to identify bundles of materials relevant to their specific role or challenge, or ways to build a personal collection of materials. Qualifications Bachelor's degree with 6+ years of experience. Experience in working with members of the media and communicating via digital channels. Experience with the PK-12 Education sector, preferably in...
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10
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Pfizer Inc. - La Jolla, CA - as a single point of accountability for the design and execution of clinical studies by closely collaborating with the Study Team Ensures appropriate data review, interpretation and reporting in collaboration with other functional groups. Reviews and tracks emerging efficacy and safety data and keeps Clinical Lead informed of changes in the efficacy/safety as they occur and take action as appropriate Presents clinical trial results internally and to the scientific community and prepare manuscripts May... designs and through application of enhanced trial design, ensures the most efficient clinical protocols are developed Is responsible for review and approval of the Informed Consent Document (ICD) Provides clinical input to the CRF design, statistical analysis plan, monitoring guidelines, and drug supply planning Supports other lines (e.g., Development Operations ) to ensure that they provide adequate support for the study and the overall development plan Works with Development Operations and AP...
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BNY Mellon - Jersey City, NJ - As part of Marketing Services, the Production Manager is primarily responsible for managing project requests for design and print. The scope of the projects varies greatly, from facilitating edits to an existing Fact Sheet, to designing a new brochure based on existing templates, to managing production of all print and electronic deliverables for major events. It s the responsibility of the Production Manager to manage the projects that come in to Production, and act as the liaison between the...
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13
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Official portal of the State of Florida - Big Pine Key, FL - Monroe County, FL - of special programs and events. Develop and maintain park interpretive displays and kiosks, coordinate staffing and operations of the nature center. *5% RESOURCE MANAGEMENT Participate in planning and conducting resource management activities including bird nesting, exotic plant control, park nursery and erosion control. Administer the park sea turtle nesting program to include identification, monitoring, evaluation and reporting of turtle nests. Schedule and train staff on proper procedure... and reports required. Research the cultural and natural resource history of the park to enhance interpretive programming. Collect and maintain cultural resource files, artifact inventories, and coordinate and participate in appropriate preservation of cultural and natural resources. Participate in non-native wildlife removal. *5% MAINTENANCE Maintain cleanliness of interpretive exhibits, displays, facilities and equipment. *35% ADMINISTRATION Oversee the day-to-day operation of the Nature Center...
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10
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Entergy - Jackson, MS - inspection cost through maximization of staff productivity and tracking expenditures within budget parameters. Monitors personnel and group effectiveness in achieving established goals. Functions as an inspector, as needed and if qualified.. Communicates with all levels of the organization, including representing the department at all meetings. Proposes process and design changes that improve station and personnel efficiency. Ensures all activities are performed within regulatory and procedural... plant operations or Equivalent Experience. (Equivalent Experience is defined as demonstrated success at the Supervisor level.) Minimum experience required of the position 5 years experience in nuclear power design, construction, maintenance, operations production, or equivalent. 3 years experience in the engineering department. Minimum knowledge, skills and abilities required of the position Meet the qualification requirements set forth in the applicable codes and standards and possess...
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28
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International Pharmaceutical Company - Northbrook, IL - pharmacovigilance specialist, ensuring the medical safety of products for the assigned Global TA and contributing to an optimal benefit-risk profile. Responsible and accountable for the timely identification and communication of emerging safety issues and safety updates of the Company Core Data Sheet, Investigators Brochure and local product labeling. This also includes responsibility for effective and regular communication with the Global TA Group Lead and with the applicable QPPV. Responsible... and accountable for the design of safety surveillance strategies, management of safety signals for drug products, both those in development and marketed products, for the collection and identification of safety signals using safety data for signal surveillance activities, categorization and prioritization of safety signals and for authoring, medical review and, as appropriate, approval of safety evaluation reports (SERs), working closely with Global Safety Science. Responsible and accountable for the risk...
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23
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Entergy - Covert, MI - Primary Location: Michigan-Covert Job Function: Engineer MRV Minimum Salary: 57000 MRV Maximum Salary: 127000.000000000000000 FLSA Status: Professional Relocation Option: Approved in accordance with the Entergy guidelines Union description/code: NON BARGAINING UNIT-NBU Number of Openings: 1.00 Req ID: 43622 Travel Percentage:Up to 25% JOB SUMMARY/PURPOSE Is the design authority and owner of the design bases. Focuses on the design of baseline modifications and design basis control... and maintenance. Design integrity is maintained through effective configuration control of design output documents (i.e., specifications, calculations, drawings, test requirements, and procedures). JOB DUTIES/RESPONSIBILITIES Maintains the design basis for each site and supports maintenance of the licensing basis. Provides cost-effective modification designs, when required, to improve plant, system or equipment performance. Provides technical support to operations, maintenance, engineering...
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29
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DESTWIN - Monroe, CT - Company Description: In today's 24/7 world, your customers expect round-the-clock access to information. They want to operate on their schedule, not yours. DESTWIN lets you use your website to provide information and services to customers any time of day or night. The DESTWIN Solution converts your website from an online brochure to an interactive website that brings existing customers back over and over again, converts prospects into new customers, and integrates with your existing systems..., JavaScript, C• Web Technologies: PHP, JavaScript, AJAX, Cascading Style Sheets,• SOAP, Web Services• Database Technologies: MySQL, PostgreSQL, MS SQL, MS Access, Oracle• Web Server Technologies: Apache• Operating Systems and Servers: Linux• System Design: Distributed Systems, Hosted Applications, Data Security The successful candidate will be capable of working in a small-companyenvironment with minimal supervision, and will accept responsibility forplanning, managing, and implementing functional modules...
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14
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Los Angeles, CA - preparation of applications (i.e., IDE, IDE supplements, Investigator Brochure) for conducting clinical investigations in U.S., Canada, Australia and EU countries. Prepare required submissions (progress reports, etc.) to facilitate the continuation of clinical studies. Participate in the review and submission activities (annual reports, change notifications, etc.) to support the maintenance of marketing approvals. Support product registrations for international markets as required. Participate in... project development teams and review plans, reports, risk management and design reviews associated with product and process projects. Other duties as assigned. Basic Qualifications: BS in Scientific discipline/engineering required. 5+ years of experience in the area of worldwide regulatory affairs in Post Marketing Assessment (both submissions and compliance) at medical device industry. Class III Medical Device experience Knowledge and experience of U.S. FDA, Canada and EU regulations...
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29
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Akebia Therapeutics - Cambridge, MA - population, safety reporting, safety risk, and accuracy in efficacy measurements. Keeps clinical/medical team appraised of observed changes to efficacy and safety data during study progression. Evaluates risk and provides innovative risk mitigation strategies in a timely manner. Ensures studies are conducted according to regulatory requirements, high scientific standards, and the final database represents the intention of the protocol design. Participate in the development of essential... documents required to support regulatory filings and study conduct as well as program level documents (CDP, Investigator Brochure). Build strong relationships with Key Opinion Leaders in concert with Akebia’s Medical / Scientific team. Establish and manage Data Monitoring Committees (DMC) and Adjudication Committees as necessary for the clinical program. Conduct pertinent literature reviews in support of project deliverables. Contribute to the preparation of abstracts, posters...
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