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Associate Manager, Regulatory Affairs Strategy - Oncology

Job in Edison, Middlesex County, New Jersey, 08818, USA
Listing for: Regeneron Pharmaceuticals, Inc
Full Time position
Listed on 2026-07-30
Job specializations:
  • Healthcare
    Clinical Research, Medical Science, Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 109900 - 179300 USD Yearly USD 109900.00 179300.00 YEAR
Job Description & How to Apply Below

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager to join our Regulatory Affairs Strategy (Oncology) team.

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.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:
  • Work Location:

    Tarrytown, NY or Warren, NJ
  • Hybrid; 4 days per week on site
Discover your role:
  • 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 requires:
  • Minimum Bachelors Degree (Advanced degree strongly preferred)
  • 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

We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or…

Position Requirements
10+ Years work experience
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