Senior Manager, Regulatory Submission Project Management

Location
Tarrytown, New York
Posted
Mar 20, 2018
Ref
12620BR
Required Education
Masters Degree/MBA
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.

Summary:

Responsible for leading and managing Regulatory Coordination staff who project manages 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, etc).

Requires minimal guidance from direct manager. Functions as a contributor as needed.
Provides support and backup to management as needed.

Duties:

Leads, manages, and develops staff who project manages Regulatory submission deliverables

Ensures effective coordination and timely delivery of submission documents to Regulatory
Operations

Provides guidance on good documentation and submission practices

Ensures facilitation of resolution of timeline issues

Ensures development and maintainence of Regulatory Coordination processes and standards in accordance with Agency regulations and guidance, and ensures staff is trained

Assists with regulatory inspection activities

Analyzes resource needs and secures additional resources as needed

Ensures regulatory system enhancement needs or technical issues are identified and solutions implemented in collaboration with CDRA Systems

Requirements:

12+ years

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

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.

Will be responsible for supervising staff.

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: 12620BR