Freelance Brochure Design Jobs : South Gate, California

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6
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Printingforless.com - Livingston, MT - PFL’s Customer Advocates are charged with helping our customers be successful. To keep customers delighted Customer Advocates consult with them on product ideas, give advice on graphic design software and manage customer projects from start to finish. Customer Advocates are empowered with the best available technology to make sure in a typical day that includes hundreds of requests that every I is dotted and every T is crossed. As a Customer Advocate, on a typical day... you might: • Offer a Graphic Designer tips for a brochure • Send a customer directions for uploading files. • Troubleshoot with a customer their graphic files • Share a customer success story at a morning huddle of 30 people. • Brainstorm with Software Developers, Press Operators and Purchasing to craft a custom solution for a new customer. This job might be for you if: You enjoy solving problems. You love taking on difficult challenges and finding creative solutions. You are patient, level-headed, and cool under pressure...
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21
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Austin, TX - contacts with current and prospective customer and other business and project partners. + Prepare and implement business development action plans for targeted markets and customers. Keep all apprised of actions planned by involved members of the corporate team. + In conjunction with corporate marketing and communications, develop major proposals, presentation and brochure materials. + Provides expert advice and direction and drive prospects through to contract award, including identifying new... development experience Expert knowledge of the operations of a construction enterprise, key competitors and industry in the assigned territory Ability to travel extensively throughout the region. Preferred Qualifications Prior experience for General Contracting company/Construction Management firm with mid-to-large scale projects of a complex nature. Proven success in business development in commercial, residential (Condo), mixed use, design-build industry. \#LI-KH1 What We Offer AECOM...
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20
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Swift Transportation - Phoenix, AZ - , hierarchy and user licenses. - Work closely with users to develop requirements, configure and test the company's CRM tools to ensure business needs are met. Lead future phase development, implementation and enhancements including the roll-out of new functionality, while focusing on delivering a world-class CRM tool. - Perform various marketing functions, such as lead generation, web-site enhancement, survey creation through analysis, mass marketing campaigns (including brochure design and communications... is maintained. - Assist senior leadership in the creation and modification of reports and dashboards; design and develop reports within company's CRM tools; utilize external tools/software as appropriate. Deliver timely, accurate and actionable business information. Act as matrixed/indirect leader to designated department personnel to create standardized sales presentations and assist in utilizing marketing tools. - Maintain a positive work atmosphere by acting and communicating in a manner...
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23
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Eli Lilly - Indianapolis, IN - , to global alignment of Phase I and II clinical studies as well as submission planning activities. Clinical Research/Trial Execution and Support Design and oversee implementation of all clinical pharmacology studies. Capabilities include understanding the unique aspects of conducting such studies in healthy volunteers and patient groups/special populations. Apply fundamental concepts of clinical pharmacology and clinical pharmacokinetics to clinical pharmacology research. Design and oversee... implementation methods for development and biomarker qualification studies. Design, create, and provide oversight for protocol development. Support development of documents for the conduct of studies in collaboration with functions and operations staff and affiliates in accordance with GCP and local requirements. Collaborate with local clinical research staff, statisticians, health outcomes research scientists and selected consultants and/or investigators in the development of protocols, and data collection...
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17
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Saint Paul, MN - sufficient resources to insure the School can achieve its mission. SPECIFIC RESPONSIBILITIES Enrollment Management Responsible for the planning, management and implementation of the marketing, recruitment and retention of students. This includes but is not limited to open houses, campus visits and tours, re-registration, brochure creation, etc. Working closely with key volunteers, coordinate the external and internal marketing efforts and initiatives that attract and retain students in sufficient... professional writing and design standards for school communications. This includes, but is not limited to: Print publications including school newsletter/magazine, marketing materials, giving program brochures, and direct mail pieces o Electronic communications including website and email o Media relations including advertising and press releases in local newspapers, local media coverage of school events. Constituent Relations Identify, recruit, and engage volunteers including: prospects, parents...
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16
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Cambridge, MA - of the new therapy to the Company Business Unit (BU) for phase 3 development Responsibilities The Director of Clinical Research will develop a disease specific global network of potential investigators and key opinion leaders for the new therapeutic before POC or ESoE trial conception to assist in trial design, as well as management and recruitment of study, analysis, interpretation and presentation of results. Design POC studies in consultation with KOLs and Company project team members. Develop... study, including regular review of safety data (including but not limited to serious adverse events) and response to safety issues. Provide leadership to the clinical function in preparation of critical documents, including but not limited to clinical protocol, clinical development plan, investigator brochure, statistical analysis plan and regulatory documents. Expand the culture of collaboration between the clinical team and partners in both research and business units by maintaining open...
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25
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Celgene Corporation - Summit, NJ - /Knowledge Required: Degree in Life Sciences (e.g., BS in nursing, pharmacy or related medical field) 7-10 years of experience in clinical research development or equivalent Minimum 1-2 yrs. experience in medical or technical writing Extensive medical/scientific and clinical research knowledge Knowledge of Medical Terminology Knowledge of protocol design, implementation and proficient at data interpretation Experience in protocol development, study report preparation, Investigator Brochure...
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25
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Pearl River, NY - biopharmaceutical industry,is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Role Description The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety. In addition... across the study and provides responses to questions on safety. Protocol design and strategy: *Provide medical input during development and updates to the clinical development plan. *Designs clinical studies to meet the stated objectives. Assures that clinical trial objectives fit with the clinical program strategy. *Ensure that documents (protocol, Informed Consent Document [ICD], etc) meet regulatory requirements and company policy and have been reviewed by IRB/IECs. *Provides medical input...
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11
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Stryker - Allendale, NJ - and department Standard Operational Procedures. For IDE/PMA studies, contribute to FDA approval process. Participate in the development/implementation/management of registries or other post approval/marketing activities as needed. Write Investigational Plan (including CRFs, labeling, etc.), with support of other depts, and consultants (e.g., statisticians, surgical advisory board, radiologists, etc.) Participate in labs to develop surgical technique guide(s) Compile Investigator brochure materials... conduct monitoring visit, when required Collaborate with Data Management and Clinical IT groups on CRF design, final CRF approval, study set-up of databases, edit checks, User Aceptance Test, data entry Quality Control (QC), data review, and SAS reports Develop and track study metrics and report study progress data to management Manage device accountability and authorize shipment of implants and instruments. Continually monitor site compliance with protocol, follow-up requirements, study data...
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Pearl River, NY - of people. Pfizer, a global leader in the biopharmaceutical industry,is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Role Description The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies.... *Communicates safety information to sites across the study and provides responses to questions on safety. Protocol design and strategy: *Provide medical input during development and updates to the clinical development plan. *Designs clinical studies to meet the stated objectives. Assures that clinical trial objectives fit with the clinical program strategy. *Ensure that documents (protocol, Informed Consent Document [ICD], etc) meet regulatory requirements and company policy and have been reviewed...
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