Principal Consultant, Labeling Strategy

Opus Regulatory, Inc.; United States; Remote; USD 210,000 - 300,000; Full time

Benefits offered by this job

Health coverage

Dental coverage

Vision coverage

Prescription drug coverage

Life Insurance

Short-Term Disability

401(k)

Job summary

Opus Regulatory, Inc. is seeking a Principal Consultant, Regulatory Affairs Labeling to manage regulatory labeling requirements for multiple projects across US and international markets.

The role involves leading labeling strategy, coordinating with client SMEs and authorities, and delivering compliant labeling content. You will drive timelines, review CCDS and TPL contents, and provide expert guidance on US, EU, and ICH requirements within a dynamic, client-focused team.

Qualifications

• 5-10+ years pharmaceutical regulatory affairs experience within Labeling.
• Bachelor’s degree; advanced degree preferred.
• Global and international regulatory experience.
• Proven project management skills.
• Ability to work independently and to be innovative in tackling operational challenges.

Responsibilities

• Manage daily regulatory labeling requirements for one or more projects across US/EU/ROW.
• Design and implement labeling strategy and operations.
• Lead preparation and update of Target Product Label (TPL) and CCDS content.
• Provide regulatory labeling expertise within client teams and with authorities.
• Support RA requirements for drug products and assess CCDS content risks.
• Develop and drive regulatory labeling timelines and deliverables.
• Represent client RA in meetings and cross-workstream activities.

Skills

Regulatory strategy

Global experience

Project management

Independent work

Education

Bachelor’s degree

Advanced degree in science (preferred)

Job description

About Opus Regulatory:

Founded in 1994, Opus Regulatory (Opus) is a consultancy providing experts in Regulatory Strategy, CMC, Labeling, and Advertising & Promotion. Our clients range from development-stage biotech companies to mid-size and large pharmaceutical organizations. Backed by Audax Private Equity, Opus has grown to roughly 120 consulting professionals across the US and UK. Our team is made up of biopharmaceutical leaders and innovators, and our mission is to provide the highest level of Regulatory Affairs consultancy in the industry—continually exceeding client expectations through excellence, partnership, and integrity.

Location: Remote | Levels: Sr. Manager - Vice President

Role Overview

The Principal Consultant, Regulatory Affairs Labeling is primarily responsible for the daily management of regulatory requirements for labeling strategy or labeling operations for one or more projects, designing and implementing labeling strategy, providing leadership to drive labeling consensus, and developing relationships with client subject matter experts and regulatory authorities. We have a robust client portfolio offering a variety of projects across therapeutic areas and regions.

Responsibilities include:

• Labeling experience across Development, Core, US, EU and Rest of World (ROW) Labeling.
• Understanding of end-to-end labeling process and systems.
• Lead preparation, review, and update content for the development and maintenance of Target Product Label (TPL), Company Core Data Sheet (CCDS), and local labeling and labeling components.
• Act as a key regulatory affairs expert within a client regulatory team, providing expertise on regulatory labeling, process, filing, best practices, etc. in conjunction with client leadership.
• Provide support and guidance to regulatory teams on RA requirements for one or more drug products by evaluating and communicating risks associated with CCDS content updates and implementation strategies.
• Uses extensive knowledge of US, EU and ICH regulatory requirements and the ability to apply knowledge both strategically and operationally to development projects and marketed product regulatory issues to support corporate goals.
• Develop and drive regulatory labeling timelines and deliverables.
• Understanding of labeling governance and process work.
• Support agency requests and documentation process for impact to labeling; participate in agency meetings as requested.
• Maintain knowledge of changing regulatory requirements and advise teams as appropriate.
• Represent the client regulatory affairs team in other client meetings or workstreams; provide support for ancillary projects.

Qualifications:

• Minimum experience: 5-10+ years pharmaceutical regulatory affairs experience within Labeling
• Minimum education: Bachelor’s degree (advanced degree in a science discipline preferred)
• Experience within many different therapeutic areas as well as labeling operations
• Global and International experience
• Proven project management skills to support the planning and coordination of labeling submissions and support appropriate regulatory inspections.
• Ability to work independently and to be innovative in tackling operational challenges.

At Opus Regulatory, we are committed to pay transparency and equitable
compensation practices.Actual compensation will be determined based on factors such
as experience, education, specialized expertise, geographic location, and internal
equity. In select circumstances, compensation may fall outside of the posted range.

US-Remote Pay Range

$210,000—$300,000 USD

Opus Regulatory is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Opus is committed to providing benefit-eligible employees with a comprehensive benefits package designed to support your health, financial well-being, and work-life balance. We offer medical, dental, vision, and prescription drug coverage for employees and their eligible family members. Additional benefits include Life Insurance, Short-Term Disability (STD), and an Employee Assistance Program (EAP), a 401(k) plan, and more. To support time away from work, we provide a paid time off package, which includes 20 vacation days, 5 sick days, & 10 paid company holidays annually.