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Category : Biotech & Pharmaceutical : Medical Writer Jobs (1 - 10)

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Medical Writer
Novo Nordisk (NJ)
...With general direction and guidance, is responsible for preparing regulatory, publication, and education documents. Ensures that accurate, quality documents are prepared on schedule. Assists other medical writers, as per project timeline and workload demands. Acts as the prime contact for...
PharmaDiversity.com (11/13/09)
 
Sr. Medical Writer
Forest Laboratories, Inc. (Jersey City, NJ)
1.Write and edit clinical documents, with competent use of English language/grammar and application of scientific standards, as lead clinical writer in assigned therapeutic area 2.Prepare high-quality clinical documents including patient narratives, clinical study reports, briefing...
PharmaDiversity.com (11/13/09)
 
Medical Writer/Sr./Principal Medical writer
ExecQuest (MA)
...The Medical Writer will write Protocols, IBs, CSRs, sections of NDAs, INDs, summary documents and annual updates. At Sr. and Principal levels of experience, may be responsible for direction, scope, and organization of specific documents. Requirements MS, PHD, PharmD or MD Minimum of 2 years...
Get Clinical Research Jobs (11/16/09)
 
Medical Writer
Pharmaceutical Associates, LLC (Raritan, NJ)
...1.Writes, reviews, and edits, as necessary, clinical protocols/amendments, annual reports to regulatory authorities, clinical study reports, regulatory documents (eg, clinical sections of anIND, dossiers, or a BLA/NDA), ad hoc clinical reports, publications, and related documents. Writes,...
Pharmaceutical Associates, LLC (09/22/09)
 
Senior Medical Writer
Human Genome Sciences (Rockville, MD)
...Human Genome Sciences (HGS)is a biopharmaceutical company with approximately 800 employees and world-class R&D and manufacturing facilities based in Rockville, MD. We have three promising products in late-stage development - one, raxibacumab, already commercialized with sales to the US,...
Human Genome Sciences (10/01/09)
 
Medical Writer II
Abbott (Dallas, TX)
...PRIMARY FUNCTION / PRIMARY GOALS / OBJECTIVES: Prepares technical documents to support both domestic and international regulatory submissions, market labeling, clinical labeling, troubleshooting guides, training aids, and customer communications for diagnostic assays and instruments....
Abbott (10/23/09)
 
Senior Medical Writer
Wolters Kluwer (Yardley, PA)
...Pharma Solutions, a Wolters Kluwer company is currently looking to add a Senior Medical Writer to their Yardley, PA office. Pharmaceutical professionals look to Pharma Solutions for exact, current and actionable information to help them better understand diseases and conditions as well as...
Wolters Kluwer (10/24/09)
 
Senior Medical Writer
Exelixis Inc. (South San Francisco, CA)
10273 Senior Medical Writer Job ID #:868 Location:South San Francisco, CA Functional Area:Biotechnology Department:Regulatory Affairs Position Type:Not Indicated Education Required:Not Indicated Experience Required:Not Indicated Relocation Provided:
Exelixis (10/30/09)
 
Principal Medical Writer
Allergan (Irvine, CA)
...In making this commitment, we work to develop an unparalleled level of insight into patients' wants and needs - and into the priorities and concerns of the medical specialists who treat them. To this end, we employ more than 50 percent of our work force in either research and development...
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Allergan (10/30/09)
 
Medical Writer
Clinical Data, Inc. (New Haven, CT)
...An emerging pharmaceutical and biomarker company that possesses a solid product pipeline including one drug candidate for which an NDA is being filed, a second Phase III drug, a solid Rx and Dx pipeline, experienced management team and Board of Directors, and an active M&A and Licensing...
Clinical Data, Inc. (11/05/09)
 
Sr. Medical Writer
Abbott (IL)
...The Senior Medical Writer is responsible for providing regulatory document support to the clinical teams, ensuring successful preparation of high quality submission-ready documents and effective implementation of the clinical writing process. Provides expertise in the medical writing for...
Abbott (11/06/09)
 
Medical Writer II
Covance (Madison, WI)
.... Writes and coordinates the development of simple to complex study protocols and protocol amendments. . Prepares scientifically valid draft and final CSRs (ie, interim and abbreviated clinical study reports to fully integrated clinical study reports), including the scientific...
Covance (11/15/09)
 

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Medical Writer
Smith Hanley Consulting - Pharmaceuticals (Berkeley Heights, NJ)
*Summary Document experience *CTD experience *Oncology preferred *Candidate needs to have medical writing experience in Phase III *Candidate should excel at data interpretation *5-7 years medical writer experience within Pharma *Degree required *Candidate will need to work onsite full time...
Climber.com (11/10/09)
 
Medical Writer/Editor
Discovery Solutions Inc. (Somerset, NJ)
...S/he would be highly experienced in medical editing of scientific/medical articles, good writing skills, also has publication planning experience, can do scientific/medical research to support article writing, has a health & pharma background, has MedEd agency experience. Experienced...
Get Copywriting Jobs (10/30/09)
 




 

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