Regulatory Affairs Senior Director Global Regulatory Leader Obesity

Career Category

Regulatory

Job Description

HOW MIGHT YOU DEFY IMAGINATION

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills experience and passion to work toward your goals At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies reaching over 10 million patients worldwide. Come do your best work alongside other innovative driven professionals in this meaningful role.

Regulatory Affairs Senior Director - Global Regulatory Leader Obesity

Live

What you will do

Lets do this. Lets change the this vital role you will support products in the Obesity Therapeutic Area. Global Regulatory Affairs (GRA) provides global regulatory leadership expertise and execution for the development registration and life cycle management of all Amgen molecules.

• To lead GRTs within Amgens GRAAS organization
• To independently develop a comprehensive regulatory strategy for one or more high complexity programs typically in late-stage development and / or with multiple indications that takes into account worldwide regulatory requirements to drive product development global registration achievement and maintenance of desired regional labeling and effective regulatory agency interactions
• To provide Regulatory leadership to cross-functional teams for high complexity programs with major Regulatory deliverables such as global original marketing applications
• Develop and implement global regulatory product strategies designed to achieve approval and target product labeling for prioritized assets in late development with highly complex development programs
• Represent GRA on the product team and other key commercialization governance bodies guide and influence the organization to achieve Regulatory objectives
• Independently develop the Global Regulatory Strategic Plan and provide regulatory input into the products Global Strategic Plan. Obtain input from the GRT members to develop a global regulatory strategy which supports product development registration and lifecycle maintenance. Identify and communicate regulatory risks
• Provide regulatory direction in the development of the core data sheet to align commercial objectives in the context of available and expected scientific data regulatory guidance and precedent
• Independently lead the planning and implementation of global regulatory filings (eg clinical trial applications marketing applications label extensions)
• Ensure consistency of evidence-based global product communication (eg regulatory submission documents)
• Monitor and assess impact of relevant global regulations guidance and current regulatory environment; advise product teams and GRT on implications of pertinent changes
• Assess regulatory mechanisms to optimize product development (eg expediting FIH studies Orphan Drug Designation Fast Track Designation conditional / accelerated approval compassionate use and pediatric plan) and ensure appropriate incorporation into the global regulatory strategy
• Clearly and succinctly communicate regulatory strategies associated risks mitigations and contingencies to the organization such that the probability of regulatory success and potential outcomes are well understood
• Lead GRTs and product teams in formal and informal communications with regulatory agencies
• Lead the approach and strategy for formal interactions with Regulatory agencies especially those which could impact the global product strategy
• Represent Amgen Regulatory on external partnership teams at the product level
• Lead regulatory process improvements and initiatives

Win

What we expect of you

We are all different yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications :

Doctorate degree and 5 years of regulatory experience in biotech or science

OR

Masters degree and 8 years of regulatory experience in biotech or science

OR

Bachelors degree and 10 years of regulatory experience in biotech or science

Preferred Qualifications :

Thrive

What you can expect of us

As we work to develop treatments that take care of others we also work to care for our teammates professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents financial plans with opportunities to save towards retirement or other goals work / life balance and career development opportunities including :

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position

Amgen is an Equal Opportunity employer and will consider you without regard to your race color religion sex sexual orientation gender identity national origin protected veteran status or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request accommodation.

#Obesity

Salary Range

216805.00 USD - 259624.00 USD

Required Experience :

Exec

Key Skills

Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 259624 - 259624