C2C :: Medical Writer - Edison, New Jersey

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<p>Dear Partners/Job Seekers<br> <br> We have a <b>Corp to Corp</b> opening for 
<b>Medical Writer in Edison, New Jersey</b>, if you have matching candidates 
please submit their profiles <strong><a 
href="http://www.job4tech.com/jobs/508908-medical-writer-at-conquest-technology-solutions-inc?utm_source=JA05-Up&amp;utm_medium=Groups-email&amp;utm_campaign=Job-Alerts";>
 here</a></strong>. </p> <p>Candidates matching the requirements will be 
contacted. </p> <p><br></p>
<p>Hi,</p> <p>Hope you are doing well,</p> <p>We are looking for a 
<strong>Medical Writer</strong> for a contract position at 
<strong>Edison,</strong> <strong>New Jersey.</strong> Please review below job 
details and send me your most updated profile, Appreciate if you can refer your 
friends or colleagues who might be looking for a job.</p> <p><strong> 
</strong></p> <p><strong>Title: Medical Writer</strong><strong></strong></p> 
<p><strong>Location: Edison, </strong><strong>New Jersey</strong></p> 
<p><strong>Duration : 8-10 Months </strong></p> <p><strong>Openings: 4 
Positions</strong></p> <p><strong>JOB DESCRIPTION</strong>:</p> <p><strong>Job 
Description for Medical Writer:</strong></p> <p><strong>Experience required: 
10-12 years.</strong></p> <p>• Prepare documents that present clinical data 
objectively in a clear, concise format. The incumbent must show competence in 
writing, editing, and reviewing Clinical Study Reports (CSRs) and other 
clinical documents like</p> <ul>
<li>Summary Documents</li>
<li>eCTD Submission Documents</li>
<li>Clinical Overview</li>
<li>Safety &amp; Efficacy reports</li>
<li>Risk Management Plan</li>
</ul> <ul>
<li>Development and updating of Investigator’s Brochures, Clinical Study 
Protocols, and other regulatory documents </li>
<li>Analysis, interpretation, and accurate presentation of information or data 
in text, table, or figure format </li>
<li>Provide dedicated scientific authoring expertise to both the development 
and research groups.</li>
<li>May need to liaise with external services and review documentation 
generated elsewhere (e.g., Clinical Research Organizations [CROs], 
subsidiaries, co-development partners), and internal support staff (e.g., for 
the preparation of tables, illustrations, and appendices).</li>
<li>Quality-checking documents for agreement between in-text information and 
the source data </li>
<li>Prepare reports, manage review cycles, and incorporate comments as 
appropriate.</li>
<li>Provision of overall medical writing support for ongoing programs</li>
<li>Scientific degree, preferably PhD, or medically qualified, or with 
equivalent relevant experience.</li>
<li>Experience (preferably 7+ years) as MW, or equivalent, or presenting 
relevant qualifications.</li>
<li>Experience Preferred in Therapeutic areas like - Oncology, Neurology, 
Cardiovascular (Not Mandatory)</li>
<li>Very good verbal and written English skills </li>
<li>High degree of accuracy with attention to detail </li>
<li>Excellent analytical and problem solving skills </li>
<li>Good level of computer literacy, in particular in the use word, excel and 
databases </li>
<li>Personal skills: good communication, presentation, flexibility, time 
management and </li>
<li>Ability to work independently and proactively within a team.</li>
<li>Ability to work on multiple projects simultaneously, while maintaining</li>
</ul> <p><strong> </strong></p> <p><strong>Qualifications:</strong></p>
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