Regulatory Affairs Manager

Recordati•Bridgewater, NJ

2d•Onsite

About The Position

This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati. Recordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives.

Requirements

Bachelor’s degree required
At least 5 years’ experience in Regulatory Affairs
Experience in a commercial-stage organization required.
Demonstrated ability to deliver quality results within a fast-paced, dynamic environment.
Knowledge of current FDA and Health Canada regulations and guidance; and knowledge of and experience with pharmacovigilance and related drug safety reporting regulations.
Ability to manage multiple priorities and regulatory submissions at different stages as required.
Strong project management skills with proven ability to drive projects through to completion.
Employee is required to have a valid driver’s license and means of transportation.

Nice To Haves

advanced degree in the life sciences preferred
Working knowledge of Veeva platform helpful but not required.

Responsibilities

Implement regulatory strategies supporting drug development and lifecycle management for US and Canada.
Review documentation and prepare lifecycle management submissions.
Review documentation and prepare drug development activity of pre-IND and IND submissions.
Liaise with regulatory authorities as needed pertaining to drug development and product lifecycle management.
Oversee submission of advertising and promotional material to the FDA as required.
Support the labeling and/or change control processes to ensure timely and comprehensive review.
Maintain labels/labeling for newly acquired and existing products in compliance with regulatory requirements and company standards.
Track Annual Report and Periodic Safety Update Reports (PSUR) schedules to ensure that required dossiers are prepared and submitted as required.
Coordinate with Medical Affairs & Pharmacovigilance to ensure timely reporting of safety data to regulatory agencies and partners.
Ensure compliance with all federal regulations regarding post-marketing reporting to the FDA and other health authorities.
Act in full compliance with all laws, regulations, and policies including adverse events / pharmacovigilance responsibilities.
Perform additional duties as may be assigned.