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Senior Associate - Regulatory Affairs (US-Remote)
full-timeThousand Oaks$88k - $110k

Summary

Location

Thousand Oaks

Salary

$88k - $110k

Type

full-time

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About this role

Career Category

Regulatory

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Senior Associate - Regulatory Affairs

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will assist the US Regulatory Leads and the Global Regulatory Team (GRT) in the Regulatory Affairs organization.

  • To coordinate and execute US regulatory submissions under the direction of the US Regulatory Lead in compliance with corporate standards and regulatory requirements.

  • To manage and execute the preparation, delivery, and electronic archiving of documentation for inclusion in US regulatory submissions

  • To assist the Global Regulatory Lead to manage GRT interactions

Key responsibilities include:

  • Assist US Regulatory Lead to support local regulatory activities (e.g. IND submissions and agency meetings)

  • Provide and maintain CTA/MA documentation support (e.g. initial filings, amendments, and periodic reports) in collaboration with US Regulatory Lead

  • Create and maintain product regulatory information and history documents through Amgen systems

  • Appropriately archive regulatory documents and agency communications

  • Collaborate with CRO’s / partners to support site initiation

  • Complete regulatory forms to support agency communications

  • Participate in GRT to support execution of regulatory strategy

  • Coordinate QC of regulatory documentation (e.g. briefing materials)

  • Provide primary authorship to routine regulatory correspondence (e.g. annual reports, investigator packages)

  • Assist in template development and maintenance

  • Respond to specific requests from and communicate relevant issues to GRT

  • Actively support regulatory compliance

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 self-starter with these qualifications.

Basic Qualifications:

Master’s degree

Or

Bachelor’s degree and 2 years of Regulatory Affairs experience

Or

Associate’s degree and 6 years of Regulatory Affairs experience

Or

High school diploma / GED and 8 years of Regulatory Affairs experience

Preferred Qualifications:

  • Strong communication skills - both oral and written

  • Ability to understand and communicate scientific/clinical information

  • Ability to collaborate with team members to tackle problems and develop a course of action

  • Cultural awareness and sensitivity to achieve global results

  • Planning and organizing abilities

  • Able to prioritize and balance multiple activities

  • Ability to deal with ambiguity

  • Ability to influence others

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of 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 that may include:

  • A 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

  • Flexible work models, including remote and hybrid work arrangements, where possible

Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

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.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

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.

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Salary Range

88,347.00 USD - 110,633.00 USD

Other facts

Tech stack
Regulatory Affairs,Communication Skills,Scientific Information,Collaboration,Planning,Organizing,Prioritization,Problem Solving,Regulatory Compliance,Documentation Management,Quality Control,Template Development,Agency Communication,Cultural Awareness,Influencing Skills

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 helped establish the biotechnology industry, and we remain on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases.

Amgen is one of 30 companies comprising the Dow Jones Industrial Average®, and part of the Nasdaq-100 Index®. In 2024, Amgen was named one of the “World’s Most Innovative Companies” by Fast Company and one of “America’s Best Large Employers” by Forbes.

For more information, visit Amgen.com and follow us on X, LinkedIn, Instagram, TikTok, YouTube and Threads.

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Special Advisory: Please be cautious of scam recruitment offers claiming to be from Amgen. Such scams may come from various sources, including fake websites and/or unsolicited emails and seek to obtain personal data or payment from victims by offering jobs that do not exist. Please be advised that Amgen would never ask for payment to progress a job application. When in doubt, please check to see if the position in question is posted on this website before applying. Additionally, please report any suspicious recruiting activity to https://complaint.ic3.gov/ and thank you for your assistance.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Biotechnology Research
Founding Year: 1980

What you'll do

  • Assist the US Regulatory Leads and the Global Regulatory Team in coordinating and executing US regulatory submissions. Manage the preparation, delivery, and electronic archiving of documentation for regulatory submissions.

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Frequently Asked Questions

What does Amgen pay for a Senior Associate - Regulatory Affairs (US-Remote)?

Amgen offers a competitive compensation package for the Senior Associate - Regulatory Affairs (US-Remote) role. The salary range is USD 88k - 111k per year. Apply through Clera to learn more about the full compensation details.

What does a Senior Associate - Regulatory Affairs (US-Remote) do at Amgen?

As a Senior Associate - Regulatory Affairs (US-Remote) at Amgen, you will: assist the US Regulatory Leads and the Global Regulatory Team in coordinating and executing US regulatory submissions. Manage the preparation, delivery, and electronic archiving of documentation for regulatory submissions..

Why join Amgen as a Senior Associate - Regulatory Affairs (US-Remote)?

Amgen is a leading Biotechnology Research company. The Senior Associate - Regulatory Affairs (US-Remote) role offers competitive compensation.

Is the Senior Associate - Regulatory Affairs (US-Remote) position at Amgen remote?

The Senior Associate - Regulatory Affairs (US-Remote) position at Amgen is based in Thousand Oaks, California, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Senior Associate - Regulatory Affairs (US-Remote) position at Amgen?

You can apply for the Senior Associate - Regulatory Affairs (US-Remote) position at Amgen directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Amgen on their website.