Temp- Editor/Senior Editor

Regeneron Pharmaceuticals
Oct 18, 2016
Oct 19, 2016
Employer Type
Direct Employer
Employment Type
Full Time
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, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including oncology, rheumatoid arthritis, asthma, atopic dermatitis, pain, and infectious diseases.

This position can be located in Tarrytown, NY, Basking Ridge, NJ or remote


The Senior Editor works to ensure the highest department document and editorial standards through providing in-depth QC and edit checks of all Medical Writing documents. This individual will train on writing Regulatory submission documents (CSRs, CSPs), and will be asked to help create parts of documents and populate tables, as well as write narratives for AEs leading to withdrawal. The Senior Editor is responsible for helping to train more junior staff, liaising with members of Regulatory Operations to ensure that information required for complex document publishing is provided on time and in the correct format, and for following up with other functional groups to ensure that material for document completion is provided on time.


The Senior Editor is responsible for the following tasks:

• Editing the following documents for spelling/grammar, consistency, correct template use and section content:

-Clinical Study Protocols

-Clinical Study Protocol Amendments

-Clinical Study Reports

-Investigator brochures

-Clinical Summary Documents

-Other documents, as needed

• Performing QC checks on Clinical Study Protocols and Clinical Study Protocol Amendments,

-This includes verifying consistency between the schedule of assessments and study description, ensuring consistency between the study schema and the schedule of events, and verifying references

• Performing QC checks on Clinical Study Reports and Clinical Summaries,

-This includes verifying consistency between hand-generated in-text tables and source tables, and between in-text numbers/ statements and source tables; ensuring consistency between discussion/ conclusion sections and results sections; and verifying reference, table, figure, and listing citations.

• Performing QC checks on IBs and IB Updates,

-This includes verifying consistency between hand-generated in-text tables and source tables, in-text numbers and source tables, in-text clinical summaries and Clinical Study Reports, and in-text non-clinical summaries and nonclinical reports


•Bachelor's degree and a minimum of 5+ years of relevant industry experience.

• Understand document content for all major Medical Writing documents and how the information needs to flow from one document to the next for a BLA/NDA/MAA submission

• Pay extreme attention to detail

• Have the ability to work independently

• Proactively identify and manage projects, requiring some but not significant guidance;

• Be a team player;

• Take responsibility for his/her own professional development

• Have the ability to comprehend key points of meetings and interactions, and follows up when necessary.

• Follow agendas for meetings; take action and produces quality written work

• Be able to juggles multiple priorities and adapt quickly to new situations and new project demands

• Escalate conflict appropriately

• Have a solid knowledge of MS WORD and Adobe Acrobat

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. 036d652fd9dc4142a409f0b9f17de7d7