Senior Regulatory CMC strategy manager

Regulatory CMC strategy manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Senior Regulatory CMC strategy manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are seeking a highly motivated and qualified regulatory CMC professional for the Global Regulatory Affairs team at ICON this is a fixed term contract initially until 31st March 2027.

The Senior Manager, CMC Strategy is responsible for global CMC regulatory strategies and activities for a large Pharma portfolio through clinical development, market launch and product lifecycle management.

The successful candidate will provide an effective and aligned regulatory CMC strategy and submission approach globally, regionally and locally.

What you will be doing

• Defining, coordinating and implementing global CMC regulatory strategies for product specific development and life-cycle activities
• Providing proactive strategic guidance to the product‑specific global regulatory and manufacturing sub‑teams for defining global regulatory CMC strategies and objectives pertaining to the development, registration, commercialization and lifecycle management of the drug product in the United States and international markets.
• The role liaises directly with the US FDA and with local regulatory teams for discussions with international health authorities and agencies for CMC-related matters.
• Negotiates with regulatory authorities during the development process to ensure submission acceptance and approval.
• Manages the CMC regulatory strategy of high quality and compliant regulatory CMC documentation (e. g., BLAs, INDs, CTAs, MAAs, Variations/Supplements and other relevant regulatory filings such as meeting requests and briefing packages) for the assigned product(s) within defined timelines as per R&D and business objectives.
• Advises on regulatory strategies, solutions to scientific problems and interpretation of results in the context of product registration requirements combined with the business need and goals.
• Facilitates the communication and flow of regulatory information (regulatory framework, scope and project timelines) to all relevant stakeholders.
• Identifies and recommends the most effective CMC regulatory strategies to assure a first-pass regulatory approval of initial application and lifecycle supplements/variations.
• Product registrations in global markets.
• Provides proactive guidance and regulatory strategies to support product teams.
• Interfaces with key functions in the preparation, review and approval of regulatory CMC submissions as assigned to product and programs.
• In collaboration with the network strategist, develops and manages timelines supporting regulatory submissions, proactively identifies risks and develops adequate risk management solutions in consultation with cross‑functional teams.

Your Profile

You will have solid regulatory affairs experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field
• The role requires an extensive experience in global pharmaceutical/biotechnological drug development and proven knowledge of the global regulatory CMC environment.
• Demonstrated experience in authoring and managing components of regulatory submissions
• Good knowledge of global regulatory requirements and demonstrated ability to function as the lead interface with FDA.

Ability to support regional and local regulatory affairs teams for interactions with regional or local health authorities (e. g., EMA, PEI, AGES, PMDA, Health Canada, etc.).

• Demonstrated ability to develop and implement global CMC regulatory strategies, resolve complex issues, and negotiate optimal regulatory pathways and outcomes with health authorities.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply.

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