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| 2 November 2009 Published weekly by Biotech Ink, LLC |
Vol 2 No 33 | |
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Open Jobs and Gigs for Medical Writers |
The jobs listed in the Biotech Ink Insider come to us mostly by word-of-mouth and direct contact with hiring managers and recruiters. If no new jobs are communicated to us in a given week, the Insider won't be published that week. See also our disclaimer at the bottom of the newsletter.
If you're a writer or editor and are getting calls about staff or contract positions you aren't interested in, please forward that job information to Susan Caldwell at caldwell@biotechink.com. We'd be delighted to publish such positions in the next issue of the Insider. |
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Senior Peer-Review Manager Bridgewater, NJ |
Our client, a strategic medical communications agency located in Bridgewater, NJ, serves global clients in the pharmaceutical and biotech industries. The agency educates the global healthcare community and enables them to make well-informed decisions regarding treatment options.
We require a SENIOR PEER REVIEW MANAGER to communicate reviewer's comments to authors and to evaluate revised manuscripts for acceptance or further revision for peer-reviewed medical journal portfolios.
RESPONSIBILITIES
Manage peer-review process
- Compile, edit and format the reviewers' comments from Editor-in-Chief and reviewers and communicate recommended changes to the authors in a professional and scientific manner.
- Evaluate the reviewers' comments for appropriateness, and completeness.
- Address any concern that the authors may have about the peer-review comments/process
Evaluate manuscript revisions
- Evaluate the author's responses to reviewers in the revised manuscript.
- Review revisions made by authors to ensure that they meet the reviewers' requirements for acceptance, and communicate further revisions if needed.
- Work closely with editors to ensure that the revised manuscript meets their requirements.
Personnel management
- Manage and collaborate with the Peer-Review Managers to facilitate the peer-review process.
REQUIREMENTS
Pharm D degree or an advanced degree in a biomedical field with 5 years relevant scientific experience.
CONTACT
The hiring company has engaged Jack Farrell & Associates ( www.jackfarrell.com) to find the winning candidate for this position. Interested candidates should provide a resume by email to joan@jackfarrell.com. |
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Contract Medical Communications Scientist Philadelphia, PA |
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The Contract Medical Communications Scientist provides medical communication expertise in the production of regulatory documentation (including regulatory dossiers, Investigator Brochures, protocols, FDA briefing documents).
Location: Philadelphia region
Hours: Mon - Fri; 8:30am - 4:45pm
Contract term: 12/22/10 (with potential for extensions)
Major Responsibilities
- Prepares regulatory documents (Investigator Brochures, clinical trial reports, NDA sections) according to agreed standards.
- Critically assesses, interprets, and accurately summarizes medical data.
- Contributes to the underlying strategy for achieving the most persuasive and effective presentation of data to the FDA to help ensure the optimal label for a product.
- Promotes and exploits global working in the preparation of clinical contributions to regulatory dossiers.
- Provides innovative advice and guidance on planning and resource forecasting for dossier and document production to enable competitive deadlines.
- Interprets and monitors current and emerging communication issues and guidelines.
- Manages contract resources through the effective use of project management skills to ensure the delivery of quality documents.
- Degree/College Major: Science background (eg, MS/PhD)
- Number of Years Work Experience Required: 3-5 years
Contact
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Medical Writer, Medical Communications New York City |
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My client, an excellent Medical Communications company in New York City is actively seeking an experienced medical writer for a full-time, permanent opportunity (On Site). Experienced writers with Medical Education or Medical Communications writing experience desired. Requirements
In-house work; this position does not allow for remote work or telecommuting.
Qualified applicants must have the following:
- A PhD, MD, or Pharm D degree in a life sciences discipline is required
- 2+ years or more of industry experience preparing & writing (manuscripts, posters, educational programs, journal articles, executive summaries, abstracts, power point, slide kits, review articles, etc)
- Oncology, diabetes, CNS, urology, cardiovascular, gastro, therapeutic experience desired (any or all or related areas)
- Experience in a variety of therapeutic areas a plus
Keywords
Sr Medical Writer, Medical Writer, Medical Director, Scientific Director, Oncology, Project Director, Medical Education, Medical Advertising, CNS, Oncology, Journal Articles, Poster presentations, Slide kits, CD-ROMs, KOL's, Abstracts, Manuscripts, Power Point
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