Assoc Mgr Regulatory Affairs

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Job description

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. The Associate Manager will be located in our Tarrytown office.

In this role, a typical day might include the following:

* Coordinate 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

* Assist in coordination and preparation for Agency meetings and associated briefing document preparation

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

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

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

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

* Exercise discretion and independent judgment in the performance of the duties described above

This role might be for you if:

* 2-3 years of pharmaceutical industry experience in regulatory affairs; experience in oncology preferred * 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

* PharmD, Ph.D or MD required

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

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