Manager- International Regulatory Lead

Career Category

Regulatory

Job Description

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

ABOUT THE ROLE

The International Regulatory Lead (IRL) Manager will provide regulatory leadership & expertise for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams to

- optimize product development and regulatory approvals in International countries develop international regulatory strategy and provide regulatory support for in-country product registrations and life cycle management.

Job Summary

The International Regulatory Lead (Manager) is assigned to lead one or more Amgen products. The product(s) assigned have medium complexity programs/strategies and medium impact to Amgen.

Provide Guidance and Leadership on mechanisms to optimize product development and regulatory approvals.

Develop the international regulatory strategy and contribute to Global regulatory plans.

Support regulatory product compliance (e.g. RIM, PMCs, ESC levels, and agency commitments).

Support and advise on the local label strategy and alignment to cCDS/reference label.

Build effective relationships and communication paths across global, regional, local and functional organizations.

Enable efficiencies and seamless execution across the international countries.

Contribute to process improvement projects, as assigned.

Key Activities

STRATEGY AND EXECUTION

Advises Global teams on regulatory implications and requirements relevant to the global clinical development/Marketing Applications plans and objectives.

Provides regulatory direction/expertise on the international regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug Designation, expedited regulatory designations, compassionate use and pediatric plan).

Under general supervision, plans regulatory submissions (e.g. clinical trial, marketing authorization applications and lifecycle management) for products within Amgen's portfolio.

Under general supervision, contributes to the development of international regulatory strategy documents (regulatory product filing plan, strategies, risks associated with the potential Agency outcomes and contingency planning, estimate likelihood of success) and communicates to others, as appropriate.

Provides and maintains CTA/MA documentation. May author documents/redact documents to support a regulatory filing.

Leads the internal discussions related with Agency meetings and in accordance with GRT strategy (and communicates outcomes back to GRT and others, as applicable).

Directs the development of the international product label by collaborating with the Labeling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance, precedents and competitor labeling.

Manages the international label submission strategy, leads the negotiation activities with cross-functional teams and is accountable for the label deviation requests and outcomes.

Supports Local Regulatory teams in triaging queries from health authorities, and where appropriate, help identify existing responses to same or similar questions, leveraging knowledge management.

Advises and supports other groups on the review of promotional and non-promotional materials, as needed.

Supports process improvement initiatives and metrics.

COMMUNICATION AND COLLABORATION

Participates as a member of the Global Regulatory Team (GRT), Evidence Generation Team (EGT), Labeling Working Group (LWG), Clinical Study Team (CST), and others, as applicable.

Shares regulatory information and implications with the GRT and other Global teams on an ongoing basis and provides advice on international considerations. Participates in LWG/ELB meetings with advice on local deviation requests.

Partners with the peers to agree on product strategy including projected submission and approval time.

Maintains regular communications with the local teams to ensure alignment on strategy and keep the countries informed of status on the product development.

Partners with peers to ensure consistency in procedures.

Builds effective relationships and communication paths across the Global and Local elements of the GRAAS function

REGULATORY RESEARCH

Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to Amgen products.

Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.

Knowledge and Skills- Scientific and Technical

Knowledge of Regulatory principles.

Working with policies, procedures and SOP’s.

Comprehensive understanding of regulatory activities and how they impact other projects and/or processes.

General knowledge of national legislation and regulations relating to medicinal products.

General awareness of the registration procedures/challenges in the region for CTAs, MAs and all lifecycle management activities.

Knowledge and experience in the international regulatory environment relevant for product area and development stage.

Understanding of drug development.

Others

Demonstrate strong team work ability.

Good communication skills - both oral and written.

Good negotiation and Influencing skills.

Ability to understand and communicate scientific/clinical information.

Ability to resolve conflicts and develop a course of action leading to a beneficial outcome.

Cultural awareness and sensitivity to achieve results across both regional, country and International borders.

Education & Experience (Basic)

Doctorate degree and 6 years of directly related experience

OR

Master’s degree and 8 years of directly related experience

OR

Bachelor’s degree and 10 years of directly related experience

Education & Experience (Preferred)

8-13 years of experience with degree and in-depth regulatory experience and/or related to the region.

In-depth knowledge of regional countries legislation and regulations relating to medicinal products.

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