Associate Manager, Regulatory Affairs Strategy

The Associate Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations.

In this role, a typical day might include:
Coordinating the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development in oncology therapeutic area, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure

Assisting in coordination and preparation for Agency meetings and associated briefing document preparation

Managing and tracking queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments

Providing representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings

Performing research to support the development of regulatory strategy for the assigned clinical development program

Maintaining knowledge of regulatory requirements up to current date, comments on draft regulatory guidance, and communicates changes in regulatory information as needed

Exercising discretion and independent judgment in the performance of the duties described above

This role might be for you if can/have the:
Knowledgeable of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices.

Experience interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred

High attention to detail; ability to organize and prioritize assigned projects according to corporate goals

Ability to work in close collaboration with colleagues in regulatory department and throughout the development organization

Proficient in written, oral, and interpersonal communications in English
To be considered for this opportunity, you must have the following:

Minimum Bachelors Degree (Advanced degree preferred)

2-3 years of pharmaceutical industry experience in regulatory affairs; experience in oncology preferred
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Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually) $108,300.00 - $176,700.00

Salary : $108,300 - $176,700