Freelance Brochure Design Jobs : California

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9
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Lennar Corporation - Eugene, OR - for executing upon stringent community schedules to meet start and closing dates. Responsible for coordinating and implementing input from division executives regarding design & engineering. Supervise, schedule and coordinate with project consultants, including architects, engineers, landscape architects, soils and environmental engineers, and other consultants to insure necessary approvals and adherence to community schedules. Delegate daily workload and priorities to staff. Report regularly as to plan... and permit status to the Director of Purchasing and Director of Construction. Assist in the processing of plans, applications or required paperwork for agency approvals and permits. Draw plot plans. Create Lot Fits. Assist in Purchasing Special Projects, including but not limited to: Creation of Floorplan Layouts, Estimating, Value Engineering, Assist in Spec Development, and Assist in Product Development. Assist in Marketing Special Projects, including but not limited to: Review Brochure Floorplans...
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Austin, TX - SR. COMPUTER SCIENTIST - SR. RESEARCH ENGINEER - EMBEDDED SOFTWARE - AUSTIN, TEXAS S SR. COMPUTER SCIENTIST - SR. RESEARCH ENGINEER - EMBEDDED SOFTWARE - AUSTIN, TEXAS Southwest Research Institute Austin, Texas, United States 1 day ago Description Job Summary: Design and develop high-reliability embedded systems software for a variety of spacecraft control avionics, ADCS systems, and power control subsystems. Perform all phases of the system lifecycle including applied research..., requirements generation, design, implementation, testing, integration, installation, and documentation. Interact and interface with clients including developing technical presentations. Field support may require travel to customer facilities. Education/Experience: Requires a BS degree in Electrical Engineering, Aerospace Engineering, Computer Science or related field with at least 7 years of experience. Must have at least a 3.0 GPA. Direct experience designing software for high reliability embedded systems...
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Johnson & Johnson - Titusville, FL - 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. PRINCIPAL RESPONSIBILITIES Strategically lead the Safety Management Teams (SMT) for assigned products. SMT responsibilities include safety surveillance (including signal detection), benefit/risk assessment and risk management activities [including Risk Management Plan (RMP) and Risk Evaluation and Mitigation... Strategy (REMS)], as well as other activities related to managing the safety profile of assigned products · Provide medical and safety expertise as the GMS representative on the Compound Development Team (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...
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Bloomberg - Glenwood, IA - , assists in interpretation and implementation of findings + Follow up on all triggers for individuals on caseload and provide appropriate assessment and referrals to other professionals for additional input. LEADWORKER: + Acts as a lead worker in the Physical and Nutritional Management Dept. in performance of diagnostic, evaluative, and therapeutic dysphagia services for residents in state ICF-ID facility. + Assists the supervisor to design, implement, and monitor the effectiveness... state offers a wide variety of career opportunities. Benefits The state offers paid vacation, sick time and holidays, a defined benefit retirement plan, health, dental, vision, and long-term disability insurance along with flexible spending accounts. For more information, please visit the executive branch employee benefits website (http://goo.gl/rHiarg) . The State of Iowa is committed to providing an outstanding employment experience. Check out thisBenefits Beyond the Paycheck brochure (https...
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Blueprint Medicines - Cambridge, MA - MIDD (Model Informed Drug Development) initiative Lead the analysis, interpretation and reporting of clinical pharmacokinetic data Develop clinical pharmacology plans (e.g. assessment of QT, food effect, ADME, DDI strategy, special populations, etc.) to support development and rapid registration of Blueprint products Plan, design, execute and report program-specific clinical pharmacology studies by working cross-functionally with Clinical Operations and Clinical Research Work collaboratively... with CROâ??s/external vendors to ensure compliance with planned study protocols, internal Blueprint quality standards and timelines Co-author regulatory documents (CTD, Investigator brochure (IB), EOP2 meetings, NDA/MAA)for submission to global health authorities Represent Blueprint Medicines at global health authority meetings Qualifications: PhD or Pharm D in Clinical Pharmacology, Pharmacokinetics, or a related discipline with a minimum of 10 years of experience in pharmacometrics and clinical...
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Johnson & Johnson - Spring House, PA - and committed to inclusion. Proud to be an equal opportunity employer. This position will serve as a Director for Immunology products in Clinical Development within the areas of Rheumatology, Dermatology, GI, and possibly other diseases. This position will have primary responsibility for various activities associated with safety monitoring and assessment for relevant clinical R&D programs and have clinical responsibility for input into regulatory documents, such as the Investigator Brochure, the Risk... Template of the Informed Consent Form, the Development Safety Update Report (DSUR), and the Risk Management Plan. In addition, this position will support protocol design, development, and execution, supervise Clinical Trials conduct, organize and participate in external advisory boards and investigator meetings, and assure that all studies are appropriately conducted per guidelines. In conjunction with a study responsible physician: The Clinical Project Scientist is a responsible member...
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The Emmes Company, LLC - Rockville, MD - communications and recommend action for implementation by Emmes, as applicable Provide medical input on safety considerations during development of protocol and associated documents Advise Study sponsor and study team on protocol development, inclusion/exclusion criteria, and eligibility questions, protocol study design and halting rules, etc Ensure the medical and scientific quality of documents such as clinical trial protocols, investigator's brochure, informed consent document, patient diaries... biomedical research. Emmes offers support for the entire process of clinical trials from study design and protocol development through data analysis and manuscript generation. PURPOSE The Medical Officer position has functional responsibility for pharmacovigilance (PV), medical consulting and review activities including protocol development activities and practical aspects of clinical trial safety monitoring. RESPONSIBILITIES Managing corporate and project related activities for existing...
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Genentech - San Francisco, CA - and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests � Provide expert contribution to the development of the product safety strategy � Take independent responsibility for risk management activities including preparation and maintenance of CCDS, labeling document maintenance (including IB), risk communications, RMP, REMS � Review of clinical protocols, study reports, Investigator's Brochure (IB), informed consent form (ICF... context of the management of Individual Case Safety Reports (ICSRs) requiring assessment. � Review of clinical study development plans and/or study protocols (and other relevant clinical trial documentation), to ensure their design is appropriate to current clinical medical practice. In addition, to ensure that the measures outlined in plans/protocols to manage defined patient risks, are appropriate/feasible to implement in the context of current clinical medical practice, and can reasonably...
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21
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Corbus Pharmaceuticals - Norwood, MA - information Serve as key analytic and safety support lead in close collaboration with the heads of medical, clinical and regulatory Support safety related activities for global clinical trials, including but not limited to review of protocols, ICFs, statistical analysis plans, safety content of Investigator Brochure, and clinical study reports Review standard design of tables, figures, and listings for safety data from clinical studies Support DMC activities as applicable Represents PV as member...
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28
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Cambridge Innovation Institute - Needham, MA - . Create and coordinate marketing and design collateral (brochures, media packs, social media, banners, digital) and website updates. Manage content marketing calendar: research, editorial, design and promotional activities across all channels. Employ existing and new marketing communications to capitalize on all revenue streams for event portfolio. Organize call lists and lead lists for team members. Clean and build database for the conference portfolio. Manage digital marketing campaigns: PPC...â??s customer targeting interface. Direct mail experience to coordinate brochure mailings with vendor. Technical skills:2+ years of LinkedIn, Google Ads, Google Analytics experience; Excel proficiency; basic HTML skills. Dreamweaver experience a plus. Database experience (SQL a plus) for marketing analysis projects and building out reports. People skills:Team player: enthusiastic about brainstorming, coming up with your own ideas, being open to input, and ready to put the plans into action. Personal...
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