|
|
|
|
|
|
|
|
|
|
|
|
Regeneron Pharmaceuticals, Inc.
Scientific Writer
Location: Tarrytown,
New York
10591
Posted on:
10/29/2009 9:00:38 AM
Postion type:
Full time
Job Code:
1607
Required Education:
NOT PROVIDED
Salary:
DESCRIPTION
Located in historic Tarrytown, New York, convenient to New York City, Regeneron is a fully integrated biopharmaceutical company that discovers, develops, and commercializes medicines for the treatment of serious medical conditions. In addition to ARCALYST® (rilonacept) Injection for Subcutaneous Use, its first commercialized product, Regeneron has therapeutic candidates in clinical trials for the potential treatment of cancer, eye diseases, inflammatory diseases, and pain, and has preclinical programs in other diseases and disorders.
With a strong research base and product focus, Regeneron is able to understand the biology of specific disease states, discover potential therapeutic candidates, and evaluate product candidates in clinical trials. Regeneron has developed several proprietary platform technologies and incorporated these into a comprehensive system to accelerate the discovery and design of fully human antibodies and move these candidates rapidly into clinical development.
We are looking for a full-time employee in the Preclinical Development and Protein Science group to author various reports and regulatory documents in support of all preclinical development programs, including INDs, Investigator Brochures, FDA Briefing Packages, sample analysis reports, pharmacokinetic and toxicokinetic reports, and other written documents, as determined by management.
REQUIREMENTS:
The ideal candidate will have at least an MS degree (or BS with appropriate experience) in a life science (biology, chemistry, immunology or biochemistry). They will have at least 4 years (MS) or 8 years (BS) of experience in writing various types of documents in support of Preclinical Development programs, including INDs, Investigator Brochures, FDA Briefing Packages, sample analysis reports, and pharmacokinetic and toxicokinetic reports, with the flexibility and passion for accepting assignments in new areas. Computer proficiency (Word, Excel, Adobe and related software) and fluency in the English language is required. The hiring level is commensurate with experience.
The position requires a strong and diverse background in the life sciences. Excellent and verifiable written and verbal communication skills are a must. Multi-faceted experience writing various scientific/technical documents in support of preclinical drug development programs, with the flexibility and passion for accepting assignments in new areas. GLP experience is a plus as is previous experience with biotechnology-derived compounds. Computer proficiency (Word, Excel, Adobe and related software) and fluency in the English language is required.
We offer a competitive compensation and benefits package to all our employees, including stock incentives, 401k with company match as well as the expected health and welfare benefits. Comprehensive relocation benefits are available, as required.
An EOE M/F/D/V
|
|
 |
|
|
|
|
|
|
|
|
|