Freelance Brochure Design Jobs : Rhode Island

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24
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eMarketingSilo - Towson, MD - relationships with current and prospective funders - Staff the Fund Development Committee Marketing & PR - Maintain LBC’s current web site and assist in creating a new one - Use social media to its maximum benefit (Facebook, LinkedIn, Twitter) - Create and distribute all marketing materials Create and distribute e-newsletters every other month Create appropriate brochure(s) - Create and send press releases for special events and announcements - Create Yearbook on CD - Create all fund... with Center Stage Arrange for behind-the-scenes tour - Plan and implement shelter visits Serve as liaison between shelters and class members Prepare and maintain sign-up sheets for dates and times for visits Communicate objectives and design an evaluation tool - Plan and implement police ride-alongs Coordinate dates with police department Serve as liaison regarding all routine issues - Make arrangements for shadowing a principle Submit class roster to BCPS with any preferences Communicate...
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19
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Leading Pharmaceutical Company - La Jolla, CA - Preferred: Bachelors or higher degree (RN, or equivalent) in field of Health Sciences or MD. Advanced degree preferred. 3+ years of experience in Oncology (and/or Immuno-Oncology), including efforts on Clinical Study Reports, Clinical trial authorship, Investigator Brochure authorship/updates, and Annual Reports. Pharmaceutical industry experience in Oncology preferred. Extensive knowledge of the clinical development process, understand concepts of Phase I-IV and principles of study design... components of IB s and regulatory submissions) in compliance with regulatory standards Serves 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...
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23
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Leading Drug Research CRO - Rockville, MD - and developmental expertise to internal PPD teams including: Indication-specific training for clinical teams Guidance during clinical trial execution Clinical data review and evaluation Investigator brochure, clinical study report, NDA/MAA document, and regulatory briefing documents review and editing Contribute to design and reporting of feasibility studies Liaise with investigators and KOLs Mentor and supervise TA clinical scientists Qualifications MD or equivalent required: subspecialty... Consulting practice Through PPDs consulting practice, the incumbent will provide industry gold standard product development plans, and top level design of clinical trial protocols that are required in the plan Thirdly, the incumbent will support the TA Head in his/her role as Therapeutic Area Strategic Teams (TASTs) leader, that role encompassing: Identifying strategic client opportunities Client pipeline analysis Identifying drug product opportunities Partner with business development...
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Novartis Vaccines - USA - Head in the administrative and operational requirements of the Cluster and in people management where appropriate Major Accountabilities Where applicable, lead matrix team of clinical colleagues (other clinicians, statisti-cians and clinical research scientists\associates), to author clinical development plans, design clinical trial protocols, clinical study reports and publications of high scientific, operational and ethical standards. Ensure consistency of data within program and across projects... 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 for individual studies, assure medical consistency within trial and across trials within program. Coordinate the preparation of the Investigator Brochure (and updates) and the Annu-al Safety Reports to Regulatory Agencies as applicable (eg IND/CTX).Accountability as principle clinical liaison to Data Monitoring Committee (DMC). Contribute to the clinical...
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Boston, MA - Location Hits: Company Description: Cosentino Group, the worlds leading producer of Silestone quartz surfaces. It focuses on the design, production and distribution of architectural and decorative solutions made from natural stone. It creates and defines leading products that are designed to provide innovative and functional solutions for the home and public spaces under the criteria of careful design, innovation and environmental respect. The group based its development on international..., distributing to over fifty countries Job Description: The Design Sales Manager is responsible for establishing Cosentino as the leader of Stone surfacing products within an assigned territory for the retail segment. He or she ensures that all retail centers, including independent dealers, architects and designers specify Cosentino products as their first choice when selling to the end consumer and / or working on a specific residential or commercial project Increase market share by elevating the...
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24
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Davis, CA - Description A City of Davis online employment application must be submitted to be considered for this position; paper applications will not be accepted. The City of Davis is currently planning a $70 million dollar upgrade including new activated sludge, tertiary filtration, solids handling, and chlorination/dechlorination facilities. This upgrade is being accomplished via Design Build and is at the 90% design stage with major construction set to begin in the spring of 2015. The City... must be submitted to be considered for this position; paper applications will not be considered. You will find the online application and brochure at the City of Davis website: . EXAMINATION INFORMATION The most qualified applicants -- based on the information provided on the application form, resume, etc. -- will be invited to participate in the selection process. Selection for this position will include an oral board interview before a qualifications appraisal panel to establish an eligibility list...
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Clinical Trial CRO - San Diego, CA - Responsibilities: Provides medical expertise on clinical drug development throughout life-cycle of compound: Supports study design, generation of study protocol, CRF, informed consent, Investigators Drug Brochure, Statistical Analysis Plan, and other study material. Provides continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria or other protocol questions, evaluates and assesses SAEs and AEs, reviews laboratory and other safety..., natural course of disease, standard of care, alternate treatment options. Contributes to and reviews Safety Management Plans, Signal Detection Plans, Pharmacovigilance Plans, Risk Management Plans including design and conduct of safety studies. Provides benefit/risk evaluations and drug safety expertise for marketed drugs, diagnostics, and devices: Evaluates spontaneous reports and literature cases. Provides individual and cumulative benefit/risk assessments. Communicates with reporting health...
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La Jolla, CA - for their contribution for the preparation of critical documents, including but not limited to clinical protocol, clinical plan, investigator brochure, statistical analysis plan, regulatory documents. • He/she will closely work in a matrix team of colleagues, including other clinicians, statisticians, clinical pharmacologists and others at an international level. The candidate will work on 2 or more projects and will support the development of clinical plans for each one. • Ensure that all activities are conducted... in compliance with relevant regulatory requirements. • Monitor and report on implementation of Global clinical initiatives in his/her group • Develop charters, resource utilization and project plans to achieve clinical project -specific goals • Implement site organizational design and develop succession planning for clinical area. • Develop people, including recruitment, retention, and career development as directed by Oncology Clinical Development Head. • Ensures development of and adherence...
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Daltile - Calhoun, GA - Please enable cookies in your browser to experience all the personalized features of this site, including the ability to apply for a job. Summer Intern - Graphic Design Job ID 2015-19820 FLSA Status NonExempt Company Mohawk Industries, Inc Business Site US-GA-CALHOUN More information about this job: Overview: Responsibilities: Assist the graphic design department with creation of point-of-Sale, brochure, print, ads and other creative material Assist in developing..., Mexico, Russia and the United States. EOE Minorities/Females/Protected Veterans/Disabled Qualifications: Currently enrolled in a four-year college degree program in Art, Design or Marketing Creative flair, originality and a strong visual sense Knowledge of Adobe Indesign, Illustrator and photoshop Familiar with PowerPoint, HTML/CSS, JavaScript, Word Press and related platforms and frameworks...
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Denver, CO - sales and marketing strategy and will be responsible for leading the sales effort to support growth. Personal Attributes: The successful candidate will have the following skills and attributes: Must be independent and a self-starter who will work on their own and take the lead on their job duties, roles and responsibilities. Must have: (1) mentoring / coaching mentality and abilities; (2) ability to lead the company from a sales and marketing perspective. Ability to design an effective... business development program that works for our business niche and provide critical feedback on existing departmental marketing efforts. Be the primary driver of new business development. Carry primary responsibility for soliciting, developing and following-up on proposals (with input from existing company Project Managers). Possess appropriate computer skills (iContact, Microsoft Office, others) to help develop marketing materials and carry out sales/marketing efforts (brochure, website, newsletter...
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