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Tequila Company - Freelance Brochure Design Job
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I have small amount of product copy that needs proofing and possibly editing. 7-8 pages depending on you format requirements. Will have continuing work after all marketing items have launched.Company profile, web, social media, brochure are where the copy will be used.
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Daiichi Sankyo, Inc. - Basking Ridge, NJ - of clinical drug development strategy. Consults with scientists in Research Labs to deliver non-clinical package necessary to support translation into clinical program. Design and oversight of Phase I first-in-man clinical trials, in addition to more advanced PhIb combination and PhII multinational clinical trials. Provides Medical input and monitoring for active trials. Works closely with Translational Science and Translational Research (Biomarker and CDx) functions to incorporate appropriate assays... and plan into the clinical program. Drafts clinical development plans and protocol profiles, and works with team on clinical protocols and investigatorâ??s brochure; Participates in creation of developmental and regulatory strategy in collaboration with Regulatory Affairs; Reviews regulatory documents from cross functional, holistic perspective; Point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters and represents clinical function at meetings...
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Johnson & Johnson - Hopewell, NJ - (CDT) and Clinical Teams Anticipate safety concerns and influence other relevant functions including Clinical teams to minimize/mitigate patient risks by active participation in the design of the clinical protocols. Be an active partner and core contributor of safety input to key regulatory or clinical documents including: - Risk management plans - Safety development plan - Clinical Trial Protocols - Informed Consent Forms (ICF) - Safety Sections of Investigatorâ??s Brochure (IB) and IB... (CSO), the Pharmaceuticals Chief Medical Officer (CMO), the Qualified Person for Pharmacovigilance (QPPV) Pharma, Senior Management, Health Authorities (HA), Prescribers and/or Patients. In compliance with legal and regulatory requirements, the MSO will also lead when appropriate, in the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen products. The MSO will primarily work in the oncology TA and may assist other TA when...
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Waltham, MA - Would you like to be part of GSKâ??s exciting oncology clinical development organization? If so, this could be an excellent opportunity to explore. As a Clinical Scientist you will be providing input on clinical and strategic issues that impact the success of our Medicine Development units. The Clinical Scientist has accountability for the oversight of conduct development, design interpretation of study results that provide data to adequately address questions concerning efficacy/effectiveness..., safety, applicability to targeted patient population, and clinical and commercial value that are consistent with the compoundsâ?? phase of development while ensuring that patient safety is of paramount concern and that regulatory requirements are incorporated through: Aid in the design, development and interpretation of results of high-quality studies Effectively interfaces with and influences across a diverse and scientifically advanced community of internal and external experts, including...
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daiichi sankyo - Basking Ridge, NJ - , and Plexxikon Inc., our small molecule structure-guided R & D center in Berkeley, CA. Job Summary: Lead Clinical Scientist or Global Clinical Leader for one or more early Breakthrough Science or Antibody-Drug Conjugate (ADC) clinical assets. Responsible for establishment and execution of clinical drug development strategy. Consults with scientists in Research Labs to deliver non-clinical package necessary to support translation into clinical program. Design and oversight of Phase I first-in-man clinical... trials, in addition to more advanced PhIb combination and PhII multinational clinical trials. Provides Medical input and monitoring for active trials. Works closely with Translational Science and Translational Research (Biomarker and CDx) functions to incorporate appropriate assays and plan into the clinical program. Drafts clinical development plans and protocol profiles, and works with team on clinical protocols and investigator's brochure; Participates in creation of developmental and regulatory...
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Galileo Learning - Oakland, CA - , professional presence. You'll be a world-class partner, working cross-functionally with other departments to create and deliver visual communications that ensure that every message stays true to the magic of Galileo. What are we looking for? Bachelor's degree or equivalent work experience. 6 years experience in graphic design for enterprise-level consumer brand(s). Significant expertise in Adobe Creative software and design, review and feedback tools; proven ability to follow through from ideation to final...Position Description Galileo is seeking an energetic, passionate, hands-on graphic designer to join our intrepid marketing team. This talented and experienced leader will be responsible for taking Galileo's visual presence to the next level, elevating a beloved consumer brand while preparing it to scale for the future across multiple channels. We value divergent thinkers who bring various experiences and viewpoints to the table at Galileo. We strongly encourage members of underrepresented...
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Story County, IA - DOT's payroll, time and absence systems presenting needs analysis and recommendations to management. Oversee the design, implementation, testing and optimization of system business processes, configuration, documentation, and reporting. Acts as the named support contact and is responsible for communicating system alerts to the affected parties. Coordinates and directs the implementation of regular system updates. You will also have the chance to give effective oral presentations to all levels... of employees, management, and like organizations. Serve as a backup to the ERP Human Capital Management Administrator and writes literature and materials to be used in programs and designs exercises to enhance training. You will develop training documentation, including How To guides, detailed design parameters and criteria, and standard operating procedures. Create instructor materials (training aids), create and maintain training presentations, course material/content and documentation. This position...
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VariQ Corporation - Rockville, MD - - brochure design, visual organization and presentation; Website support - VariQ internal and external website information architecture and content strategy; Business Development graphic support - proposal graphic conceptualization and creation; Business Development SME support - proposal content writing re user-centered design and UI/UX expertise. High-quality presentation support - for corporate events and client meetings; Technical Demo team support - interactive design, wireframes, web user...Overview VariQ is looking for a UX/Graphic Designer with experience in visual design, user-centered design, information architecture, content strategy and user interface design. The Designer will be a part of a dynamic team dedicated to providing high-quality solutions to federal clients. Additional Information: Location: VariQ office in Rockville, MD Salary: Dependent upon experience Security Clearance: None Available: ASAP Responsibilities Marketing material preparation...
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NC REAL ESTATE COMMISSION - Raleigh, NC - and timeliness of prepared publications and management of publication inventory. Duties and Responsibilities Essential Duties and Tasks Work is performed under the supervision of the Executive Director and/or Chief Technology Officer. Produces and manages digital media content and print publications for the Commission. Produces email, banner and website design using HTML, and CSS. Designs graphics, videos, layouts and the like for print, web, email, and digital publications, for in-house software... with translators, graphic designers, artists, photographers, printers and others as necessary for creating a publication and oversees compliance with terms of contract once the contract is approved by the Chief Technology Officer and/or Executive Director. Performs periodic updates, coordinates publication of "Real Estate Licensing in North Carolina," "Questions and Answers" brochures, "Real Estate Commission" brochure and other Commission publications. Proofs and submits new communications...
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Collegeville, PA - ROLE SUMMARY Primary purpose is to serve as a Clinician for the Group B Streptococcus Vaccine program to assist in the global clinical development of a GBS conjugate vaccine. The clinician medical monitor is accountable for providing medical and scientific expertise and oversight for specific 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... to sites across the study and provides responses to questions on safety. Leads/Contributes to protocol design and strategy: Provide medical input during development and updates to the clinical development plan. Designs or contributes to design of 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...
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