Senior Associate Regulatory Affairs
US - California - Thousand Oaks - Field/Remote, United States
Career Category
RegulatoryJob Description
HOW MIGHT YOU DEFY IMAGINATION?
You’ve 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 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 in the creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced regulatory lead.
- Assist U.S. Regulatory Lead to support regional regulatory activities
- Provide and maintain IND/BLA documentation support (e.g. annual reports, amendments) in collaboration with U.S. Regulatory Lead
- Create and maintain product regulatory history documents and appropriately archive all regulatory documents and agency communications
- Review regional component of the Global Regulatory Plan and provide input to operational deliverables
- Ensure compliance with submissions to regulatory agencies
- Support U.S. Regulatory Lead in review of HA interaction activities
- Collaborate with CRO’s / partners to support site initiation, as applicable
- Coordinate collection of functional documents in support of regulatory applications
- As appropriate participate in GRT to support execution of regulatory strategy
- Coordinate QC of regulatory documentation (e.g. briefing packages)
- Provide primary authorship to routine regulatory correspondence (e.g. annual reports, investigator packages)
- Prepare regulatory packages and cross-reference letters to support investigator initiated studies
- Approve drug shipment for Amgen and Investigator Initiated Studies
- Complete regulatory forms to support agency communications
- Provide regulatory support to Commercial, Medical and Clinical departments through cross-functional interactions in brand and therapeutic area teams
- Support process improvement initiatives, standards development, and metrics
- Assist in template development and maintenance
- Respond to specific requests from and communicate relevant issues to GRT
- Develop Regulatory Position with teams
- Actively support regulatory compliance
- Support the development and execution of GRT goals
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 partner with these qualifications.
Basic Qualifications:
Master’s degree
Or
Bachelor’s degree & 2 years of Regulatory experience
Or
Associates degree & 6 years of Regulatory experience
Or
High school diploma / GED & 8 years of Regulatory experience
Preferred Qualifications:
- Master’s degree in a biology, life science, health science curriculum, or regulatory science with biology curriculum
- Regulated industry, science or clinical practice experience
- Timeline management
- Strong communication skills - oral and written
- Organizational skills
- Ad hoc meeting support
- Agendas, minutes
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.
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.
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
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
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.
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.
.Salary Range
89,063.00 USD - 109,121.00 USD ApplyJob Profile
Field/Remote
Benefits/PerksAnnual bonus program Career development Career development opportunities Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Health benefits Life and Disability insurance Personal growth Professional and personal growth Professional growth Remote work Remote work arrangements Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans Well-being support
Tasks- Collaboration
- Communication
- Create and submit regulatory documents
- Documentation
- Ensure compliance
- Ensure compliance with submissions
- Process Improvement
- Regulatory Compliance
- Regulatory support
- Support regional regulatory activities
Biology Biotechnology BLA Career Development Clinical Practice Collaboration Commercial Communication Communications Compliance Development Documentation Execution IND Insurance Management Metrics Organizational Process Improvement Project Management QC Quality Control Regulatory Affairs Regulatory Compliance Regulatory Documentation Regulatory Documents Regulatory strategy Sales Strategy Teams
Experience2 years 6 years 8 years
EducationAssociate Associates Bachelor's Degree DO GED High School High school diploma Master's
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9