Arizona Medical Writer Jobs

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  • Medical Writer(Detroit, Michigan)

    Medical Writing Position Available Looking for a Writer with a Masters level concentration in English Writing. This individual would be responsible for writing medical articles, preparation of grant applications and assist in medical research. Hours are flexible and the pay is $20 per hour. Interested applicants should email their resume and two short examples of writing to DeborahKaplan at dkapla...
    Full job description at Monster

    Posted Fri 29th March

  • Senior Medical WriterWHC Inc(Central, New Jersey)

    Significant career opportunity for strong Senior Medical Writer with at least 2 years’ experience Innovative, independent, newly established US branch of a UK-based 28-years global group of agencies in medical education and regulatory is recruiting an experienced Senior Medical Writer. With seven of top ten global pharmaceutical companies as clients, and growing by four new clients a year, the nee...
    Full job description at Monster

    Posted Thu 4th April

  • Medical Writer, SeniorMediMedia(Philadelphia, Pennsylvania)

    At Complete Healthcare Communications (CHC), we are building to be the very best strategic medical communications company and medical content partners in the world. We have committed ourselves to achieving this mission by leading the industry in quality, service, and innovation in the field of publication planning. We know that our colleagues are the reason we are where we are today, and will cont...
    Full job description at Monster

    Posted Tue 23rd April

  • Medical WriterClinicalRM(Frederick/Hagerstown, Maryland)

    Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at USAMMDA. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Medical Writer for the Frederick, Maryland area. RESPONSIBILITIES: Write, review, e...
    Full job description at Monster

    Posted Tue 30th April

  • Medical WriterCardiovascular Research Foundation(New York City, New York)

    Who we are: The Cardiovascular Research Foundation, headquartered in New York City, has been dedicated to research and education in the broad subspecialty of interventional cardiology and endovascular medicine for over twenty years. By establishing the safe use of new technologies and pharmacologic agents, CRF has played a major role in the remarkable advances in survival and quality of life being...
    Full job description at Monster

    Posted Wed 1st May

  • Medical Writer / Senior Medical WriterTakeda Pharmaceuticals(Chicago, Illinois)

    Please note that the requirements specified in this posting are the basic qualifications required for the Medical Writer position; however, job title will be dependent on the candidate's level of experience in those requirements. OBJECTIVE: Executes medical writing activities for projects in accordance with applicable US and international regulatory regulations and Takeda requirements under the su...
    Full job description at Monster

    Posted Thu 2nd May

  • Medical Writer PrincipalGenzyme Corporation(Boston, Massachusetts)

    . This position is responsible for providing high quality clinical documentation to the Genzyme Rare Disease business. The purpose of this job is to create and to manage creation by others of any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data o...
    Full job description at Monster

    Posted Mon 6th May

  • Nonclinical Medical WriterAclairo PDG Inc.(Vienna, Virginia)

    Job Summary: The purpose of this job is to create, without supervision, any type of nonclinical regulatory document (e.g., protocol, study report, nonclinical and ADME sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present nonclinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced...
    Full job description at Monster

    Posted Wed 8th May

  • Medical WriterClarity Consultants(Northern, New Jersey)

    Medical Writer We are working with our client in finding two Medical Writers. In this role, you will act as the medical writing expert responsible for the research, writing and editing of study level and submission level documents. You will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Additionally, you will assist in the develo...
    Full job description at Monster

    Posted Thu 2nd May

  • Technical Writer- Bio Medical ProductsAdecco Technical(Seattle, Washington)

    Our client a leader in manufacturing test equipement and bio medical products is in need for the following resource-. Title: Technical Writer Location : Everett, WA Duration : 6months plus ( Contract to hire) Pay rate : 40/hr on W2 or DOE Only locals to Seattle , WA who can work for any employer on W2. This is a contract to hire position Responsibility: Develop technical user and service manuals f...
    Full job description at Monster

    Posted Fri 10th May

  • Statistician/SAS,Outcome Research,Data Manager,Drug Safety,Medical Writer,Document SpecialistTechData(Northern, New Jersey)

    TechData is hiring Outcome Research Statistician, Biostatistician(Some can be remote), SAS Programmers (Some can be telecommuting), Drug Safety Specialist and Trial Safety Manager, Medical Data Manager,Clinical Data Manager, Document Specialist in Central and Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData...
    Full job description at Monster

    Posted Wed 15th May

  • Senior Medical WriterEnvivo Pharmaceutical(Boston, Massachusetts)

    Senior Medical Writer Job Objectives and Tasks: Write, edit and/or manage the production of high quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications. Act as a member of clinical trial teams Act as a documentation specialist in clinical trial teams Supervise outsourcing ...
    Full job description at Monster

    Posted Thu 16th May

  • Medical WriterIntegrated Resources, Inc.(Central, New Jersey)

    Remote Contract Medical Writer Location: Home-based (company office located in Holliston, MA) Job Type: Full-Time Duration: 3-6 months contract (possible contract extension) Compensation: Open to discussion Summary of Job Responsibilities: · Write Patient Narratives for phase III oncology trials · Adhere to sponsor’s template and format for all narratives · Meets critical project deadlines and sub...
    Full job description at Monster

    Posted Mon 20th May

  • Medical WriterA-Line Staffing Solutions(Chicago North, Illinois)

    Medical Writer II Prepares technical documents to support both domestic and international regulatory submissions. Incorporates text, graphs, charts, tables and statistical analysis. Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. 3-5 years exp. Basic Qualifications: Minimum 1 year scientific publications writing experience. Ability to understand medical data ...
    Full job description at Monster

    Posted Mon 20th May

  • Appeals Writer Specialist For Full Time Day Shifts At St. Vincent Medical Center, Little RockConifer(Little Rock, Arkansas)

    Description Description As a part of the Tenet and Catholic Health Initiatives family, Conifer Health Solutions is a leading healthcare business process management services provider working to improve operational performance for more than 600 clients so they can support financial improvement, enhance the patient experience, and drive value-based performance. Through our revenue cycle management , ...
    Full job description at Monster

    Posted 3 days ago

  • Statistician&SAS(remote),LSH–Oracle Clinical,Medical Writer,Clinical Data Manager,Biomarker Trial HeTechData(Northern, New Jersey)

    TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
    Full job description at Monster

    Posted 3 days ago

  • Senior Medical WriterWorldwide Clinical Trials(Austin, Texas)

    Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi...
    Full job description at Monster

    Posted 3 days ago

  • Scientific Writer (Medical / Healthcare)Creative Circle(Chicago, Illinois)

    Position: Scientific Writer (Medical / Healthcare) Location: Northern Suburbs Status: Freelance Estimated Duration: 1 Year + Starts: Interviewing Now Rate: DOE 　 Job Description: Our medical industry client is looking for a Scientific Writer with experience in the healthcare or medical fields to join their team for a long term freelance assignment. You will be responsible for writing and managing ...
    Full job description at Monster

    Posted 2 days ago

  • PSUR Safety Medical WriterConsignMed(Philadelphia, Pennsylvania)

    ConsignMed, a Niche Clinical Staffing Company since 2003, and rated by Diversity Business as one of the fastest growing companies in the US is seeking a PSUR Safety Medical Writer. The required skill sets/experience includes the following: Candidates must have experience working with Safety reports and must have hands on experience authoring of PSUR reports. Ability to interpret, analyze and clear...
    Full job description at Monster

    Posted Tue 21st May

  • Senior Medical WriterSanofi US(Central, New Jersey)

    Job Summary: The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced medical writer with d...
    Full job description at Monster

    Posted Fri 17th May

Arizona Job Search Tip

Arizona's job outlook is strong and shows no sign of slowing. The largest employers in Arizona are in Services, Trade and Construction, according to the Arizona Department of Commerce. Despite lags in other areas of the country, manufacturing employment continues to rise in Arizona. Arizona also has a large and growing tourism industry for those who want to share their love of Arizona with others.

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