Associate Director Inspection Management (GCP)

The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.

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

Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.

• Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.
• Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.
• Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.

Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.

This Role May Be For You If Have

• Advanced knowledge, understanding and application of GCP, and/or GVP
  
  

guidelines including the management of significant/complex quality issues

and compliance activities.

• Extensive experience with participating in, and supporting, Regulatory
  
  

Agency Inspections of Investigator Sites, Sponsors and Clinical Research

Organizations (CROs) in a GxP environment, including inspection

preparation, facilitation, and follow-up.

• Effective management of interpersonal relationships, stakeholder
  
  

engagement, and collaborations.

• Demonstrated ability to interface and collaborate effectively with other
  
  

Managers and Directors within, and external to, the organization.

• Extensive experience in providing training and presenting information on
  
  

key quality and regulatory compliance information.

To be considered for this opportunity we are looking for:

Bachelor's degree with a minimum of 10 years of relevant

healthcare/pharmaceutical industry experience.

• Experience working in either a quality/compliance role (e.g., Quality
  
  

Management, Quality Assurance etc.), or in a Clinical Development role

with expertise and/or transferable skills related to Good Clinical Practice

(GCP), and/or Good Pharmacovigilance Practice (GVP).

• Experience in training, supervising, line management, mentoring and
  
  

development of staff, and leading a small team

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.