Regulatory Associate: Average Salary in Chicago, IL in 2024

Our client, a prestigious Am Law 100 firm, is seeking an Associate Attorney to join their projects team! This team is recognized as Band 1 in all relevant categories by Chambers. Address regulatory aspects of developing, financing, buying, and selling a diverse range of energy projects across the co...

Our Senior Manager/Associate Director of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance personalized medicine. At Tempus, we are building a regulatory team that will adopt creative approaches as...

Our Senior Manager/Associate Director of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance personalized medicine. Check all associated application documentation thoroughly before clicking on the ap...

Keeps abreast of regulatory compliance issues and assist in developing new Regulatory Department procedures, as needed. Prepare, assemble, review and/or evaluate, publish and archive new ANDA and life cycle management regulatory submissions in accordance with local regulatory requirements and guidel...

In this vital role you will assist the US Regulatory Leads and the Global Regulatory Team (GRT) in the Regulatory Affairs organization. To coordinate and execution of US regulatory submissions with the US Regulatory Lead in compliance with corporate standards and local regulatory requirements. Assis...

For the expansion of our team, argenx is looking for an Associate Director of Medical Writing to contribute to the development of complex clinical, nonclinical, and safety documents for regulatory submissions. Author clinical content and project manage SME contribution of regulatory documents to dev...

The Chicago office of Kirkland & Ellis LLP is currently seeking a mid-level associate with outstanding credentials and qualifications to join our Healthcare & Life Sciences group. Additionally, the group handles everyday regulatory considerations that significantly affect healthcare and life science...

Our Senior Manager/Associate Director of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance personalized medicine. At Tempus, we are building a regulatory team that will adopt creative approaches as...

We’re looking for an entry-level Regulatory Specialist to be responsible for the daily functions of the Regulatory Affairs Department, the coordination of report filings to federal, state, provincial, and local agencies, as well as the data submissions to customers and agencies. Assists with the mai...

The Chicago office of Kirkland & Ellis LLP is seeking an experienced associate with outstanding credentials and qualifications to join the regulatory practice of our Investment Funds Group. ...

As an Associate, Reliability Compliance you will support Invenergy’s Reliability Compliance program for the entire Invenergy fleet with an emphasis on electricity generation regulatory requirements (NERC & IESO) associated with cyber security and real timeoperations. Based out of our downtown Chicag...

RSM's AML/Regulatory Compliance group is currently seeking a strong resource to join our fast growing Risk Consulting practice at the Senior Associate level. This position will lead and deliver regulatory compliance internal audits, assessments, model validations and other services at client locatio...

The Global Regulatory Affairs Office (GRAO) is responsible for overseeing the enhancement of our risk management and controls, remediation of regulatory and audit findings and the administration of regulatory affairs, including establishing a centralized and sustainable connection point for global r...

SummaryA career in our Balance Sheet Management practice, within Financial Risk and Regulatory services, will provide you with the opportunity to help business leaders embed a proactive and dynamic risk management capability and mind set into their corporate business practices. You’ll help build too...

The Manager, Regulatory Affairs, is responsible for leading and managing all regulatory activities related to both new and existing products, ensuring they meet local, regional, and global compliance requirements in alignment with company policies. The Regulatory Affairs Manager will provide expert ...

Responsible for a product(s) or products with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director, or Director), in the development & execution of the regulatory strategy. Assures that regulatory strategies defined with...

Analysts will report to a Compliance Manager and assist with ensuring the firm complies with the Bank Secrecy Act, USA PATRIOT Act, anti-terrorist financing, sanctions, industry anti-money laundering, and securities laws and regulations. Interactive Brokers is looking to hire two Trade Surveillance ...

Compliance and Risk Management Specialist. Heartland Human Care Services (HHCS) is seeking a proactive and detail-oriented Compliance and Risk Management Specialist to join our team. Reporting to the Director of Compliance and Risk Management, you will play a critical role in safeguarding the organi...

Working with other Regulatory Affairs Directors, develops and maintains an inventory of all compliance and regulatory requirements related to the organization's major risk areas, including: academics, career services, enrollment management, licensing, student finance, student services. The Senio...

You will lead the Regulatory Affairs department and report to the Vice President of Global Quality and Regulatory Affairs. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance w...

The Senior Director/Director of Regulatory Affairs, Biopharma, will provide regulatory guidance for (Bio)Pharma product development and tech transfer, especially biosimilars. The successful candidate will develop regulatory strategies for projects and portfolios in BioPharma, contributing to the tra...

Senior Director of Regulatory Affairs, Specialty Pharma, will be responsible for leading regulatory strategy for specialty pharma products, especially combination products in development and life cycle management, including A/NDA products and biosimilars. Over 10 years related experience in product ...

The Senior Director/Director of Regulatory Affairs, Biopharma, will provide regulatory guidance for (Bio)Pharma product development and tech transfer, especially biosimilars. The successful candidate will develop regulatory strategies for projects and portfolios in BioPharma, contributing to the tra...

Act as the liaison between quality departments (clinical, supplier quality, and post-market surveillance) as well as product division.Responsible for analysis of problems identified by leadership and independently recommending and implementing solutions....

Directs technological research by studying organization goals, strategies, practices, and user projects. Completes projects by coordinating resources and timetables with user departments and data center. ...