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The Cyber-Spy.Com Usenet Archive Feeds Directly From The Open And Publicly Available Newsgroups These Group And Thousands Of Others Are Available On Most IS NNTP News Servers On Port 119. Cyber-Spy.Com Is NOT Responsible For Any Topic, Opinions Or Content Posted To These Or Any Other Newsgroups. This Web Archive Of The Newsgroups And Posts Are For Informational Purposes Only. Message-Id: <031013120047137.NP32138@jobcircle.com> Newsgroups: alt.bestjobsusa.computer,alt.bestjobsusa.computer.jobs,alt.bestjobsusa.jobs.offered From: KEV1@judge.com (JobCircle.Com) Reply-To: KEV1@judge.com Subject: US-NJ: Somerset-Medical Writer Date: Mon, 13 Oct 2003 12:00:47 GMT NNTP-Posting-Host: 207.106.112.162 NNTP-Posting-Date: Mon, 13 Oct 2003 08:00:47 EDT Organization: JobCircle.com (jobcircle.com) ************************************************************** JobCircle.com - Careers, Content and Community for Technology professionals in the Northeastern United States! Jobcircle.com provides resume submission, classified searches, eLearning, hundreds of career development articles, tech news, and more to tens of thousands of Technology professionals in your area - visit us today at http://www.jobcircle.com! !!! Voted a TOP 50 Career Web Site in 2002 by CareerXRoads !!! ************************************************************** Please reply to KEV1@judge.com with your resume! Job Title: Medical Writer Job Location: NJ: Somerset Pay Rate: open Job Length: over 1 year (contract) Start Date: 2003-10-13 Company Name: The Judge Group, Inc. Contact: kev1@judge.com Phone: 732-346-9100 Fax: 732-346-9101 Description: If you have Call Intercept on your phone, please provide your password with your response/resume OR deactivate the service during your career search with Judge. Thank you in advance for helping us provide a more timely response to your interest in our job posting. Judge is looking for someone for a Medical Writer: Writes clinical study reports (CSRs) for US Medical Research-managed phase III and IV studies. Collaborates with other members of the project team to gather information, establish time frames and priorities, and delineate individual roles in preparation of documents. Drafts, writes, and edits CSR according to client's guidelines, standards, SOPs. Ensures that statistics validate clinical interpretation of data. Ensures that clinical message as conveyed by medical product leader is presented accurately and clearly in CSR. Ensures that statistics are presented accurately; prepares appropriate in-text tables to present data. Performs due diligence to ensure that all material included in the CSR is scientifically, clinically, and statistically valid. Responsible for filing of completed CSR and appendices in repository. Writes clinical study outlines and protocols. Drafts documents in collaboration with study team. Ensures protocol meets all regulatory and stylistic guideline, contains an appropriate statistical analysis plan, and will provide data needed for writing the CSR and scientific publications. Ensures protocol language accurately and clearly describe study objectives and methodology. Prepares clinical development plans, and other clinical documentation as required. Supports activities of USSP. Collaborates with SP counterparts to ensure timely preparation of publications plans. Writes abstracts, manuscripts, other materials as needed. Remains current with client and competitors' publications. Identifies potential publishing opportunities based on upcoming, current, and completed clinical studies. Serves as resource for in-house and outside writers and editors as needed. Supports medical writing group efforts and goals. Other responsibilities: Attends departmental and group meetings as scheduled. Supervises work of freelance writers/editors as necessary. Key requirements: Must be willing to work 37.5 hr/week on-site as a long-term (18 months +) contractor. Education requirements: Minimum of bachelor's degree in scientific or clinical (e.g. nursing, pharmacy) discipline; advanced degree or training preferred 1-3 years experience in pharmaceutical, scientific, clinical, or medical communications field. Experience writing CSRs/ protocols/SOPs/other types of clinical study documentation. Experience writing abstracts or manuscripts for scientific/clinical journals preferred Skills and knowledge requirements. Interest in actively participating in development of new medical writing group within a growing scientific publications department. Able to adjust to changes, take on new challenges, and develop professionally. Demonstrated ability to communicate effectively orally and in writing. Demonstrated ability to write English clearly, and accurately. Must be able to meet deadlines for delivering work. Able to understand, evaluate, and interpret scientific, clinical, and statistical data. Strong interpersonal skills; must be able and willing to work effectively with other members of the department, writing group, and project team. Able to organize and prioritize work and keep accurate and up-to-date records; must be detail-oriented, but also flexible in adjusting to changing priorities and schedules. Must be able to work independently as well as cooperatively. Knowledge of medical research, pharmaceutical industry, drug development, and regulations pertaining to research, clinical trials, ethical conduct. Proficient using Microsoft Office (Word, Excel, Powerpoint), performing literature searches, using Internet. Applicant must be a U.S. resident or currently able to legally work in the U.S. Please refer to Job code 29273 when responding to this ad. For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/372212.html to apply online. ************************************************************** For fastest processing of your resume, this employer asks that you apply to this job using the URL above. ************************************************************** Go Back To The Cyber-Spy.Com Usenet Web Archive Index Of The alt.bestjobsusa.jobs.offered Newsgroup |
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