21 August 2009                 Published weekly by Biotech Ink, LLC Vol 2 No 24

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Inside the Insider
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Convention Coverage: A Taste of Medical Journalism 
by Karen Rappaport, MD
 
Finding medical writing jobs when you are new to the field of medical writing isn't easy. As a relatively new medical writer, I was delighted when a friend recommended me for a freelance assignment. The job was to write articles for a daily newspaper published for a 5-day medical conference.
 
First, a word of explanation. At medical conferences, the number of lectures and symposia is usually huge--no one can attend all of them. For this reason, sometimes companies are hired to write and publish a newspaper that covers the main conference events. The newspaper is delivered to the attendees each morning, beginning on the second day of the conference. The companies that publish these newspapers aren't necessarily local, so they hire local freelance medical writers to do the writing.
 
I had a telephone interview with a representative from the publishing company. Much to my chagrin, I found myself talking about my experience years ago, as the editor of my high school newspaper! Yet, some of the rules I learned about journalism back then applied to this job, and I was offered the position.
 
The publisher sent me their writer's manual, which included rules about grammar, punctuation, and reminders to avoid using passive voice. The manual also described how to write in the inverted pyramid style, which allows the reader to get the gist of the article by only reading the first few sentences.
 
A few days after I received the manual, the publisher recruited some advance writers, and I offered my services. The advance writing team was to write articles before the meeting, based on medical abstracts and online interviews with some of the authors. The articles ranged from 300 to 700 words, and each summarized two to four abstracts. For the first time since high school, I tried to write in the inverted pyramid style.
 
Writing for a medical conference newspaper requires the writer to decipher medical information in a field they don't necessarily know much about. Despite my medical background, I still had to look up abbreviations that the abstract authors assumed their readers would know. Wikipedia was very handy for these searches, and was also a quick source of background information. I also used PubMed's archive of peer-reviewed biomedical journal articles; it was an invaluable resource for referencing earlier works by the abstracts' authors.
 
The day before the conference began, the publisher asked me to summarize some more abstracts written by the speakers. Once again, I sat down at my computer to draft an article.
 
The difficult part of the assignment--writing articles under time pressure, on site, without prior information--was yet to come. What was it like to work as a medical writer at one of these conferences?
 
As it turned out, my job during the conference was mostly to get a few good quotes and capture new information presented at the meeting. After the first day, I amended the article I had written the night before to include some quotes and new information. I submitted my article, and it was published without any major corrections.
 
Although I didn't get to work as much on site at the convention as I'd hoped, I'm still very glad I accepted the assignment. I'd recommend this sort of work to freelance medical writers living near cities with a major convention center. Not only did I gain a little experience in medical journalism that I'll add to my resume--I even had a good time doing the job!
 
About the Author
_______________________________________________________________________
 
Karen Rappaport holds an MD and a PhD in health services research, and is a board-certified anatomic and clinical pathologist. She is embarking on a new career as a medical writer, which will draw on her expertise in medicine and public health. Her current work focuses on preparing manuscripts ready for publication in the peer-reviewed medical literature. In the foreseeable future, Karen plans to broaden her areas of medical writing expertise into other genres, including regulatory documents. 

Karen Rappaport, MD, PhD
Medical Writer
Write for the Pharm, LLC
Tel: 650-315-4411
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.
Training Opportunity for Technical (and Medical?)Writers:  Job Seeker Boot Camp
 
From the Society for Technical Communications web site:
 
As a technical communicator, you know that access to the right information is crucial. STC's Job Seeker Boot Camp was "designed to help you find jobs during these difficult times." It's a free service to STC members, and non-members can register for this special service for $65 until 31 December 2009.
 
What you get for your registration fee: 
  • Access to the STC Career Center
  • Articles with advice for job seekers
  • Access to 2 podcasts
  • Access to STC's salary database

Note from S Caldwell: I have no experience with this service, and am including it in this issue of the Insider for your information. Check it out at your own risk. If you use this resource, please let me know your opinion of the service. If I get feedback, I'll let you know what your medical writer colleagues thought of it in a future issue of the Insider.

Senior Medical Writing Specialist
Foster City, CA or Durham, NC
 
This role can be located in either Durham , NC or Foster City, CA.  (Telecommuting is not an option ~ sorry.) 
 
Specific Responsibilities and Skills for Position:
 
Experience writing CTD submission summaries and overviews, briefing documents, development plans, as well as CSRs and IBs. Knowledge of antiviral and/or cardiovascular TAs a plus.
 
Essential Duties and Job Functions:
 
Prepares a wide range of regulatory documents, including clinical study reports, Investigator Brochures and Annual Updates, as well as more complex CTD summaries and regulatory responses, in-line with regulatory requirements and Gilead internal document standards. Contributes to other non-regulatory medical writing activities as required. Participates in submission teams providing advice/guidance for optimal presentation of data for achievement of document objectives. Leads document timeline/resource planning within the submission team. Works collaboratively with functional contributors (clinical, biometrics, virology etc), ensuring all source information / data are appropriately reported in terms of accuracy, completeness and scientific interpretation, and in accordance with project timelines. Medical writing activities are performed independently with little direction from Associate Director / Director level. Leads the compilation of final documents and appendices coordinating clinical, biometrics and regulatory contributions. Leads/contributes to development work in relation to document standards, continuing MS template development and other aspects of document management. Provides submission team contact point regarding requirements for regulatory documents. Participates in both group and moderately complex Company-wide process improvement and development initiatives.
 
Knowledge, Experience, and Skills:
 
Specific pharmaceutical: Typically requires a BA degree and minimum 10 years of relevant experience within clinical R&D or regulatory affairs such as pharmaceuticals/biotechnology, which includes 5 years of relevant experience in a medical writing/clinical submissions environment preparing documents for regulatory submissions. General scientific: Typically requires a BA degree and minimum 10 years of relevant experience or a MS degree and minimum of 8 years of relevant experience or a PhD, MD or DVM degree and minimum 4 years of relevant experience. Demonstrated success in the preparation of regulatory documents particularly at the individual study report level. Highly developed and proven medical writing skills. Excellent verbal communication skills. Knowledgeable of regulatory document requirements/guidelines. Understands moderately complex document management, authoring and publishing tools and their applicability for workflow efficiency. Well-developed computer skills including proficiency in Word, Powerpoint and Excel. Use of project management tools and graphics packages also desirable.
 
If you are interested in being considered for these positions or if you know someone who is qualified, please contact me.  I'd appreciate any referrals.
 
Best regards,
 
John Pandes
Senior Staffing Consultant
Gilead Sciences, Inc.
O: (650) 522-5599
Scientific Medical Writer
Northern NJ
 
Industry: Major Pharmaceutical Company
 
Salary
: $75-$105K
 
Description:

The Scientific Writer is the medical writing expert responsible for the research, writing and editing of regulatory documents. The incumbent will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Responsibilities will include assuring quality and timely preparation of clinical documents across all therapeutic areas, including clinical study reports, clinical study protocols, investigator's brochures, and clinical summaries and overviews.

Qualifications:

Requirements: Bachelor's degree or equivalent, with at least six years experience in scientific discipline and a minimum of four years in Medical Writing. Master's degree, PhD, or equivalent with a minimum of two years previous industry experience. Demonstrated working knowledge of scientific principles. Excellent written and oral communication skills in English. Familiarity with all phases of medical research and ability to learn new medical concepts quickly. Familiarity with statistics and experimental design. Ability to summarize complex data and identify relationships.

Must have Clinical Study Reports and Regulatory submissions experience.

Interested candidates please send resume to:
 
Medical Writer, Medical Communications (Multiple Positions) 
San Francisco Bay Area
 
Medical Communications Agency:

Medical Director- must have PhD, PharmD, or Md degree and medical communications agency experience

Sr. Account Manager

Account Manager

Speakers Bureau Manager

Pharma Advertising Agency:

Account Supervisor or Group Account Supervisor

Anyone interested or if you know anyone looking, please contact me via
email at shannonp@sheilagreco.com.

Best Regards,

Shannon Peryea
Vice President, Executive Recruiting
Sheila Greco Associates, LLC
174 State Hwy 67
Amsterdam, NY 12010
(518) 843-4611 ext. 252
shannonp@sheilagreco.com
www.sheilagreco. com
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