5 Executive Director, Regulatory Affairs Jobs in Los Angeles, CA
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Executive Director, Regulatory Affairs
$215k-293k (estimate)
Full Time | Scientific Services
3 Months Ago
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Biospace is Hiring an Executive Director, Regulatory Affairs Near Los Angeles, CA
HOW MIGHT YOU DEFY IMAGINATION?At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared missionto serve patientshas driven our status as one of the worlds preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge partnerships that advance the biotechnical and biopharmaceutical science that can turn the tide of serious, life-interrupting illnesses.
Executive Director of Regulatory Affairs LiveWhat You Will DoLets do this. Lets change the world. In this vital role as Executive Director of Regulatory Affairs, you will direct regulatory affairs activities within an assigned disease area, ensuring compliance with applicable laws and regulations. You will also provide strategic direction and leadership to the regulatory affairs team.
The Executive Director of Regulatory Affairs is a product facing role that leads a designated part of the Inflammation and Rare Disease Global Regulatory Therapeutic Area in the Global Regulatory Affairs organization. This role will report into the Vice President, Global Regulatory Affairs
Responsibilities
Basic Qualifications
The annual base salary range for this opportunity in the U.S. is $259,141 - $300,862
In Addition To The Base Salary, 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
We recruit the best talent, build an environment that facilitates career growth, and provide staff with the opportunity to make significant contributions for patients and our business.
We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.
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.
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.
Executive Director of Regulatory Affairs LiveWhat You Will DoLets do this. Lets change the world. In this vital role as Executive Director of Regulatory Affairs, you will direct regulatory affairs activities within an assigned disease area, ensuring compliance with applicable laws and regulations. You will also provide strategic direction and leadership to the regulatory affairs team.
The Executive Director of Regulatory Affairs is a product facing role that leads a designated part of the Inflammation and Rare Disease Global Regulatory Therapeutic Area in the Global Regulatory Affairs organization. This role will report into the Vice President, Global Regulatory Affairs
Responsibilities
- Provide management and leadership of regulatory strategy within the assigned therapeutic area for Global Regulatory Affairs
- Direct the development of global and United States regulatory therapeutic area and product regulatory strategies to drive product development, global registration, achievement and maintenance of desired regional labeling, and effective regulatory agency interactions
- Provide regulatory expertise and guidance to therapeutic area commercialization teams and other governance bodies
- Advise the Global Regulatory Leader (GRL) in the development of global regulatory strategies and the United States Regulatory Leader (USRL) in the development of US regulatory strategies, including precedence, risk management and contingency planning
- Conduct management review and approval of Global Regulatory Strategic Plans
- Conduct review and approval of key documents for regulatory submissions
- Contribute to the target product label, core data sheet, and regional labeling
- Monitor, assess and communicate to staff impact of relevant global regulations, guidances, and current regulatory environment
- Advise on global health authority interactions and participate on core regulatory and cross-functional teams to ensure effective agency interactions
- Work externally to influence regulatory legislative environment in line with Amgen policy priorities for the therapeutic area
- Oversee and participate in licensing/acquisition due diligence and other activities in partnership with Amgen licensing groups
- Provide managerial leadership & direction to staff within assigned area allowing appropriate prioritization of resources to achieve goals
- Recruit and retain talented regulatory affairs professionals.
- Provide coaching, mentoring, and career development of staff
- Ensure staff are compliant with Amgen corporate and departmental training
- Communicate and ensure alignment of global functional and cross-functional goals and objectives
- Demonstrated ability to lead teams
- Strong communication skills - both oral and written
- Ability to understand and communicate scientific/clinical information
- Comprehensive understanding of regulatory activities and how they affect projects and processes
- Demonstrable ability to set organizational direction & champion change and continuous improvement
- Proven ability to anticipate and mitigate against future strategic issues & uncertainties
- Ability to resolve conflicts and develop a course of action leading to a beneficial outcome
Basic Qualifications
- Doctorate degree & 6 years of regulatory affairs experience OR
- Masters degree & 10 years of regulatory affairs experience OR
- Bachelors degree & 12 years of regulatory affairs experience AND
- 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
- Inspire: Create a connected, inclusive, and inspiring work environment that empowers talent to thrive
- Accelerate: Enable speed that matches the urgency of patient needs by encouraging progress over perfection
- Integrate: Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders
- Adapt: Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results
The annual base salary range for this opportunity in the U.S. is $259,141 - $300,862
In Addition To The Base Salary, 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
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
We recruit the best talent, build an environment that facilitates career growth, and provide staff with the opportunity to make significant contributions for patients and our business.
We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.
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.
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.
Job Summary
JOB TYPE
Full Time
INDUSTRY
Scientific Services
SALARY
$215k-293k (estimate)
POST DATE
06/25/2024
EXPIRATION DATE
07/25/2024
WEBSITE
biospace.com
HEADQUARTERS
CERRITOS, CA
SIZE
50 - 100
FOUNDED
1985
CEO
KI CHUL CHA
REVENUE
$10M - $50M
INDUSTRY
Scientific Services
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About Biospace
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The job skills required for Executive Director, Regulatory Affairs include Regulatory Affairs, Leadership, Biotechnology, Communication Skills, Alignment, Managing People, etc. Having related job skills and expertise will give you an advantage when applying to be an Executive Director, Regulatory Affairs. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Executive Director, Regulatory Affairs. Select any job title you are interested in and start to search job requirements.
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