Associate Scientific Writer

Tarrytown, New York, US
Jul 13, 2018
Required Education
Bachelors Degree
Position Type
Full time
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.

Full-time employee in the Preclinical Development and Protein Sciences group to independently author clinical bioanalytical reports, bioanalytical research/experimental reports, precision medicine, and protein chemistry sciences documents. Provides assistance to Scientific and Sr. Scientific Writers in reviewing and performing a Quality Control (QC) check for various scientific reports and regulatory documents in support of all preclinical development programs, including INDs, pharmacokinetic and toxicokinetic reports, and other written documents in support of preclinical development programs, as determined by management.


• Independently author clinical bioanalytical reports

• Independently author research/experimental bioanalytical reports

• Independently author protein chemistry sciences documents

• Independently author precision medicine documents

• Provide editorial and QC review for IND written and tabulated summaries

• Adhere to a report process flow and alert appropriate personnel if a process change or delay occurs

• Communicates clearly and in a timely manner to a wide range of people

• Takes direction well and assumes responsibility for getting the work done

• Update and keep current the PCD Writing Group Sharepoint website

• Abide by GLP, GCP, and all company SOP's pertinent to the position

• Keeps current with software and regulatory guidances necessary for execution of job responsibilities

• 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

• Bachelor's degree in a life science (biology, chemistry, immunology or biochemistry)


• 0-2 years supporting nonclinical/clinical development programs

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.