Temp-Regulatory Submission Project Management Associate

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.


Responsible for project management of Regulatory submission deliverables such as INDs and amendments, CTAs and amendments, BLAs and amendments/supplements, MAAs and variations in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH). Provides support and backup to management as needed.


•Creates and maintains Submission Plans (Table of Contents, Timeline, and responsibility matrix)

•Coordinates submission documents (routing documents for review and uploading into the EDMS)

•Conducts kickoff, submission core team, and line function meetings

•Provides guidance on good documentation and submission practices

•Facilitates the resolution of timeline issues

•Provides requested submission documents to partners and CROs

•Maintains and tracks regulatory commitments

•Assists with reviewing and developing departmental procedural documents in accordance with Agency regulations and guidance

•Prepares and submits CAS and USAN applications

•Assists with regulatory inspection activities

•Identifies and communicates regulatory system enhancement needs or technical issues to management and CDRA Systems

•Bachelor's Degree (preferred) and 5-7+ Years

•Requires strong knowledge of applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH).

•Requires eCTD knowledge.

•Project management skills desired.

•Can work independently, ability to multitask, self-motivated, well organized, detail oriented, able to prioritize, works effectively under pressure, and has excellent written and verbal communication skills.

•Strong knowledge with MS Office applications and Adobe Acrobat is required. Strong knowledge with MS Project and electronic document management systems (eg, SharePoint) is desirable.

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. 2129b1d0403a438f6326