Subject: Opportunity
From: Lisa Rinderknecht <rinderknecht -at- HRCONSULTANTS -dot- COM>
Date: Thu, 14 May 1998 10:25:13 -0700

Dear TECHWR-L Subscriber,

We are contacting you in hopes that you may know of an individual who
would be well-suited for the attached career opportunity. Based on your

interest in technical writing, you may know of someone interested in
exploring a medical writer opportunity within a pharmaceutical company.
Please review the attached opportunity. If you are aware of interested
candidates, please feel free to forward this message; you may also
contact us directly at 619-673-3390 for more details. Thank you for
your time and consideration.

Senior Medical Writer

Our client, located in San Antonio, TX, is a pharmaceutical company
specializing in oncology and providing contract research services in
oncology. This public organization currently has the following

The incumbent will be responsible for the format, content, presentation
and organization of regulatory documents for NDA?s and INDA?s, including
clinical study reports, summary documents, clinical protocols and
investigator brochures. Accountabilities include: working with clinical,
biostatistics, regulatory affairs and project management personnel to
ensure that pertinent information is included in documents, assisting in
the preparation, writing and editing of medical research study reports
for inclusion in regulatory submissions and/or journal publications,
attending relevant conferences/seminars to keep abreast of medical
writing issues within the industry, and making relevant presentations as
needed. The senior medical writer will also identify and manage
appropriate medical writing contractors and perform editorial reviews of
material as necessary.

Preferred Candidate Profile
B.S./M.S. in Medicine, Chemistry, Biology, Pharmacology or related
field. Additional education and training in technical writing,
regulatory requirements for submission to FDA required. Knowledge of
the drug development and commercialization process. Journalistic
skills, including writing, editing, layout, design and graphics.
Experience planning, conducting and analyzing clinical trials.

This professional opportunity offers a competitive salary, benefits
package and a dynamic work environment. If you or anyone you know may
be interested, please mail/fax your resume to:

HRG, Inc. Dept. MW/KW
17055 Via Del Campo, Suite 200
San Diego, CA 92127
Phone: (619) 673-3390
Fax (619) 673-6203
E-mail: JOBS -at- hrconsultants -dot- com

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