Freelance Brochure Design Jobs : Houston, Texas

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24
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Novartis Vaccines - USA - (other clinicians, statisticians and clinical research scientists \ associates), to author clinical development plans, design clinical trial protocols, IBs, clinical study reports and publications of high scientific, operational and ethical standards. Ensure consistency of data within program and across trials Bear primary responsibility and accountability for quality and timeliness of clinical trial synopses, protocols and all clinical trial documents Address scientific and medical issues related... trial activities (includes but not limited to, scientific and medical issues as well as subjects safety) Responsibility for Data Listing review for the medical portion of data listing, assure medical consistency within trial and across trials within program Coordinate the preparation of the Investigator Brochure (and updates) and the Annual Safety Reports to Regulatory Agencies as applicable (eg IND/CTX) Contribute to the clinical sections of regulatory files, including labelling (SmPC...
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28
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Barakat Inc. - Cambridge, MA - The Graphic Designer creates and updates physical and online materials for showcasing Barakat's identity and the organization's programs, projects, and events. To apply, submit resume, cover letter, and portfolio to internships@barakatworld.org. Do not use the internships.com submission system. Responsibilities Principal Responsibilities -Design and update materials such as the brochure, newsletter, monthly updates, flyers, banners, posters, invitations, calendars, etc. -Work with the...
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26
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Sterling Life Sciences - California - 1 and 2) br 3) Lead preparation of clinical sections of all relevant documents and regulatory filings (Investigator brochure, IND, study reports, etc.) br 4) Interact with key opinion leaders to ensure implementation of latest clinical thinking and guidelines into the clinical development plan br 5) Serve as medical and technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contract resources br 6) Interact in collaborations... with strategic partners br 7) Represent the company at scientific, commercial and financial community meetings and presentations, as well as other public relations opportunities br 8) Be responsible for clinical development plan in highly competitive therapeutic areas br 9) Provide input/review study start up documentation, e.g. CRF design, source data verification plans based on protocol specifications br 10) Attend and provide science support for investigator and consultant meetings and other study...
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27
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American Biotechnology Company - Basking Ridge, NJ - development or equivalent Skills/Knowledge Required: Oncology/Hematology experience is strongly preferred Minimum 2 yrs. experience in medical or technical writing Extensive medical/scientific and clinical research knowledge Knowledge of protocol design, implementation and proficient at data interpretation Knowledge of clinical trial design, basic statistics, pharmacodynamics and pharmacokinetics Experience in protocol development, study report preparation, Investigator Brochure preparation, IND...
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24
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International Consumer Products Corporation - New York City, NY - role you will: Assist in developing mission, objectives and 3-year innovation strategy for the category with a specific focus on the brand and develops plans to achieve them Manage Key Brand Innovation Initiatives: drives the brand by working with cross functional team (Product Development, Package design engineering, Design, Creative, Purchasing, Manufacturing, Finance) progress and tracks the development of all product initiatives and ensure timely launch within cost/margin objectives... marketing groups to provide timely communication of product development process and ensures that all market needs are met in a cost effective and strategic manner Proactively drive the cross functional team in all aspects of the development and delivery of product innovation Manage the brochure and package creative process developing creative briefs, ensuring global agreement on creative direction and liaising with the Creative Agency brochure creative development. Develops advertising briefs...
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International Pharmaceutical Company - Northbrook, IL - 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... to the Global TA Group Lead with regards to the design and successful implementation of medical safety strategies for drug products within the Global TA, by authoring, reviewing and, as appropriate, approving medical-scientific reports, safety analyses and evaluations and ensuring cross-functional implementation and follow-up with the appropriate stakeholders in and outside GMS and the GPV organization. For specific Astellas products assigned to the Global TA, accountable as a product responsible...
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AMD-Molecular - Illinois - . Actively participates as a member of the cross-functional project team. Participates in assessing performance data generated by R&D/Business Teams prior to initiation of the clinical study. Acquires a basic understanding of the principles of the assay and/or instrument and “hands-on” knowledge and skills in performing assigned assays or operating instruments. Prepares clinical plans that meet product design goals, intended use, regulatory requirements, divisional operating procedures..., and Clinical Research work instructions. Prepares clinical protocol, clinical brochure, case report forms, informed consents, and other required documents for clinical studies. Identifies and qualifies clinical investigators and clinical sites. Proposes and negotiates budgets for clinical studies. Initiates payments to clinical sites. Obtains and reviews all required essential documents necessary for study initiation. Collaborates with Statistical Support with the collection and statistical...
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Johnson & Johnson - Raritan, NJ - Assessment (MSA), 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 contribute to and supervise, when appropriate, the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen Research & Development, LLC products. The Medical Safety Officer provides..., Safety Sections of Investigator’s Brochure (IB) and IB addenda, Clinical Study Reports (CSR), Annual Safety Reports (ASR), Integrated Safety Summary (ISS) and Summary of Clinical Safety (SCS) for NDA/BLA/MAA filings, Periodic Safety Update Report (PSUR), Core Data Sheets (CDS), and Informed Consent Form Risk Template. The MSO will work across the GMS TAs to align and improve common processes including providing strong leadership and a harmonized approach across clinical teams for safety data...
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20
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RefrigiWear - Dahlonega, GA - or on Websites Fulfills brochure/catalog requests made through the Website (mailings to customers) Designs Website graphics based on team needs using Adobe programs Lays out and produces quarterly newsletter and other internal communications pieces, such as posters and t-shirt designs Produces various customer-specific price lists per year (knowledge of InDesign tables critical) as well as customer-specific brochures Provides support for graphic design projects in the department as directed...POSITION DESCRIPTION: The Production and Graphic Designer will be instrumental in carrying out design and production work for a variety of projects, including brochures, presentations, price lists, Web graphics, Website updates and photo/graphics retouching. The Production and Graphic Designer will also play a critical role in the distribution of materials, including fulfilling Web orders for brochures and other direct mail campaigns. As a member of a small but professional in-house...
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6
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Novartis Vaccines - USA - Contributes to the project strategy and to the Clinical Development Plans Primary responsibility (with Cluster team) for: Preparing trial protocol, amendments and informed consent form, taking ac-tive part in study design internal discussion/meetings Coordinating the preparation of other clinical trial documents including: CRF, diary cards, study manuals, IND updates, clinical summaries Maintaining accurate and up-to-date information in project management sys-tems and trial specific tracking... systems (Clin Track) Management of overall timelines for internal study document approval and trial allocation Ensuring that appropriate documents are available to regional teams for timely submission to Ethics Committees and/or Regulatory Authorities ac-cording to local requirements Supports Cluster Physician/Clinical Scientific Lead in preparation of investigators brochure...
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