Temporary Associate Scientific Writer

Location
Tarrytown, New York
Posted
Mar 20, 2018
Ref
10692BR
Required Education
Other
Position Type
Contract
Position Summary

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Summary:

Full-time employee to support the Preclinical Development department. Assists with writing nonclinical study reports, including pharmacokinetic and toxic kinetic reports. Manages the document review process for nonclinical study reports and collaborates with authors to reconcile comments.

Duties:

• Assists Scientists with writing the nonclinical and clinical pharmacology study reports using the approved report template
• Manages the review process for nonclinical study reports
• Collaborates with authors to reconcile comments
• Updates and maintains nonclinical document templates
• Adheres to a report process flow and alerts appropriate personnel if a process change or delay occurs
• Communicates clearly and in a timely manner to a wide range of personnel
• Takes direction well and assumes responsibility for completing assignments
• Abide by GLP and all company SOPs pertinent to the position
• Keeps current with software and regulatory guidance's necessary for execution of job responsibilities

Requirements:

Proficient in preparing accurate, written reports
• Basic background in the life sciences
• Strong attention to detail, establishing priorities and scheduling
• Excellent interpersonal and communication (verbal and written) skills
• Demonstrate ability to work effectively in a flexible environment
• Ability to work independently, take initiative and complete tasks to meet deadlines
• Computer proficiency (Word, Excel, Adobe and related software) and fluency in the English language is required
• Basic understanding of the eCTD and the drug development process is a plus
• GLP experience is a plus as is previous experience with biotechnology-derived compounds

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Requisition Number: 10692BR