Regulatory Affairs Manager - Oncology and Regulatory Promotion
$112.74k - $152.54kAmgen Inc. (IR)
Career Category Regulatory Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Regulatory Affairs Manager - Oncology and Regulatory Promotion What you will do Let’s do this. Let’s change the world. In this vital role you will be responsible for formulating and communicating the regulatory promotional position for approved and/or pipeline Oncology products and disease state. Responsibilities: Provide strategic direction for product and disease communications and associated activities by interpreting current regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public Serve as a regulatory advertising and promotion lead for approved and/or pipeline Oncology product and disease state Ensuring deliverables are consistent with the product label, compliant with US FDA regulations and guidance, and adhere to Amgen SOPs and policies Identifying opportunities and challenges that impact US product strategy based upon evolving competition, regulatory environment, and clinical data Experienced in evaluating appropriate levels of evidence to make product claims Mentor Manager level promotional reviewers 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 OR Master’s degree and 2 years of industry experience Bachelor’s degree and 4 years of industry experience Associate’s degree and 8 years of industry experience High school diploma / GED and 10 years of industry experience Preferred Qualifications: 2 years experience in Oncology Experience in interpretation of government regulations, policies, and guidance Strong clinical data analysis skills Ability to use judgement and data to formulate and communicate positions on complex issues Experience collaborating within large cross-functional teams What you can expect from 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. Salary 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. Salary Range 112,744.00USD -152,536.00 USD Benefits 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 where possible. Refer to the Work Location Type in the job posting to see if this applies. 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. Sponsorship Sponsorship for this role is not guaranteed. Equal Opportunity Employer 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. 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. Salary Range 112,744.00USD -152,536.00 USD Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit and follow us on #J-18808-Ljbffr Amgen Inc. (IR)
- Amgen seeks a Regulatory Affairs Manager for Oncology and Regulatory Promotion to shape regulatory positions for oncology products in the US. You will lead strategic communications, ensure FDA-compliant promotions, and mentor junior reviewers. Collaborate with Clinical...Suggested
- Arcutis Biotherapeutics Inc is seeking a Director, Regulatory Affairs Advertising & Promotion to lead regulatory review for promotional, disease-state and non-promotional materials, ensuring compliance with FDA guidance and internal policies. The role interfaces with Commercial...Suggested
$133.08k - $180.05k
...on four therapeutic areas – Oncology, Inflammation, General Medicine... ...Trade Compliance Senior Manager LIVEWhat you will doLet's make... ...and other applicable global regulatory authorities. As the primary escalation... ...risk management, regulatory affairs, audit, law, or a related...SuggestedFull timeWork at officeWorldwideFlexible hours- Director, Global Regulatory Lead - Obesity & Related Conditions (Chronic Weight) Join Amgen... ...With our focus on four therapeutic areas - Oncology, Inflammation, General Medicine, and... ...Team (GRT) and represent Global Regulatory Affairs and Strategy (GRAAS) on cross‑functional...SuggestedFlexible hours
- Arcutis Biotherapeutics Inc. in California is seeking a Senior Manager Regulatory Affairs Advertising & Promotion to lead the Promotional Review Committee (PRC) processes and ensure materials stay compliant with SOPs. You will coordinate 2253 submissions with Regulatory...Suggested
$179.98k - $243.51k
...on four therapeutic areas -Oncology, Inflammation, General Medicine... ...a wide variety of legal and regulatory issues concerning complex... ...of the healthcare community (managed care organizations, hospitals... ..., reviewing and approving promotional, educational and support programs...Full timeContract workFlexible hours- ...Description Job Description Job: Manager, Quality Systems and... ...inspection management, and support regulatory inspection readiness across... ...GxP functional areas. Promote a culture of quality and compliance... ...Clinical, CMC, Regulatory Affairs, and other GxP functions to...Full timeWork at office
$118.24k - $159.97k
...With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and... ...established quality standards. They implement and manage QA systems, coordinate audits, and lead... ...compliance with cGMP practices and regulatory requirements.Provide leadership and...Full timeRemote workFlexible hoursShift workDay shiftAfternoon shift- ...) team, you will report to the Chief Trade Compliance Counsel, manage a Corporate Compliance Engineer, and provide indirect leadership... ...to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is...Minimum wagePermanent employmentFull timeWork experience placementLocal areaWorldwide
$136.74k
...on four therapeutic areas -Oncology, Inflammation, General Medicine... ...as an adviser to staff and managers, offering guidance on the... ...adherence to applicable laws, regulatory standards, and internal procedures... ...Drug Administration (FDA) promotional compliance standards;...Full timeInternshipWork at officeRemote workFlexible hours- ...focus on four therapeutic areas Oncology, Inflammation, General... ...a wide variety of legal and regulatory issues concerning complex contracting... ...the healthcare community (managed care organizations,... ...Analyzing, reviewing and approving promotional, educational and support...Full timeContract workRemote workFlexible hours
- ...With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and... ...while transforming your career. SENIOR MANAGER, PORTFOLIO ANALYTICS & STRATEGY Lets do... ...owning Amgens Probability of Technical and Regulatory Success (PTRS) process across the R&D portfolio...Flexible hours
- ...’s toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease, we reach millions... ...the lives of patients while transforming your career. Senior Manager, Value & Access Analytics Cross Portfolio & Innovation What you...Flexible hours
- ...development and execution of business by building and proactively managing strong export and import compliance programs in accordance... ...approval of visitor and travel requestsLiaise with Government regulatory agencies on import or export compliance issues and respond to...Permanent employmentFull timeWork experience placementWork at officeLocal area
- ...biotechnology company in Thousand Oaks is seeking a Director, Global Regulatory Lead for its obesity programs. This role involves developing... ...should have significant experience in global regulatory affairs, particularly in obesity and related conditions, coupled with...
$129.23k - $174.84k
...focus on four therapeutic areas -Oncology, Inflammation, General... ...selection, IND-enabling packages and regulatory submissions. This role will... ..., and decision frameworks.Promote high scientific standards, quality... ...direct authority, and manage multiple priorities in a matrixed...Full timeContract workFlexible hours$173.99k - $235.4k
...on four therapeutic areas -Oncology, Inflammation, General Medicine... ...has multiple components: management of in vitro cardiac safety and... ..., clinical translation, regulatory strategy, and advancement of... ...Supervise scientific staff, promote their development and ensure...Full timeFlexible hours- Kite Pharma seeks a Director of Submission Project Management to lead strategic planning and execution of major regulatory submissions globally. You will coordinate clinical data readiness, cross-functional teams, and governance to ensure timely, compliant filings. Prerequisites...
$199.06k - $269.32k
...toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions... ..., BAI PODs, Access, Field Effectiveness, Data Science, Data Management, Legal, Privacy, Compliance, Procurement, and external data...Full timeFlexible hoursShift work- ...With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and... ...patients while transforming your career. Manager Contracts & Pricing Strategy - EVENITY®... ...Finance, Accounting, Legal, Government Affairs, Trade & Distribution, Commercial Data and...Contract workFlexible hours
$196.61k - $266k
...on four therapeutic areas -Oncology, Inflammation, General Medicine... ...engagement, and performance management. The ability to influence... ...practices while ensuring legal and regulatory compliance.What we expect of... ..., affiliation, digital, or promotional data.Experience leading...Full timeFlexible hours3 days per week- ...With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and... ...investor engagement, annual reports, and regulatory filings including: Assist in the... ...minutes. Familiarity with and use of board management and online D&O questionnaire platforms...Work at officeFlexible hours
$262.53k - $355.19k
...four therapeutic areas –Oncology, Inflammation, General... ...opportunity to transform LDL-C management across the U.S.... ...Market Access, Medical Affairs, R&D, Digital, Data & Analytics... ...comply with applicable regulatory, legal, and ethical standards while promoting a highly compliant...Full timeFlexible hoursNight shift- Amgen in Thousand Oaks, CA seeks a Manager to lead United States Regulatory Strategy for General Medicine. You will shape regulatory strategy, interactions... ...pivotal trials. Ideal candidates bring regulatory affairs leadership experience in the US, strategic thinking, and...
$211.41k - $286.02k
...on four therapeutic areas -Oncology, Inflammation, General Medicine... ...and lifecycle management of Amgen products while ensuring... ...patient safety, worker safety and regulatory compliance across our global... ...Device Engineering, Regulatory Affairs and EHSS.Influence...Full timeRemote workFlexible hours$148.72k - $201.2k
...focus on four therapeutic areas -Oncology, Inflammation, General... ...transforming your career.Senior Manager, Instructional Design and Labeling... ...closely with Human Factors, Regulatory Labeling, Packaging... ...and regulatory expectations.Promote strong documentation practices...Full timeFor contractorsFlexible hours$107.45k - $145.37k
...focus on four therapeutic areas -Oncology, Inflammation, General... ...Environmental, Health & Safety (EHS) Manager and help shape a world-class... ...champion risk management, regulatory compliance, and continuous... ...influencing decision-making, and promoting employee engagement through...Full timeWork at officeFlexible hours$155.75k - $210.72k
...With a focus on four therapeutic areas — Oncology, Inflammation, General Medicine, and... ...career. Competitive Intelligence Senior Manager, Global BiosimilarsLet’s do this. Let’s... ...experience working with proprietary technical, regulatory and financial data sources (i.e....Full timeFlexible hours$133.87k - $181.11k
...focus on four therapeutic areas -Oncology, Inflammation, General... ...transforming your career.Senior Manager, Global Security - ATO CampusWhat... ...risk management; develop and promote site-specific crime... ...chain security programs and regulatory requirements, including TSA,...Full timeContract workLocal areaFlexible hours- Amgen is seeking a QA Manager in Thousand Oaks, CA, to oversee the quality assurance team, ensure products meet quality standards, and... ..., a strong background in cGMP, and the ability to interact with regulatory authorities during inspections. #J-18808-Ljbffr Amgen
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Manager - Oncology and Regulatory Promotion. Be the first to apply!
- regulatory & compliance manager Thousand Oaks, CA
- head compliance Thousand Oaks, CA
- compliance manager Thousand Oaks, CA
- regulatory affairs director Thousand Oaks, CA
- compliance director Thousand Oaks, CA
- regulatory manager Thousand Oaks, CA
- manager regulatory affairs Thousand Oaks, CA
- regulatory contract Thousand Oaks, CA
- regulatory scientist Thousand Oaks, CA
- regulatory engineer Thousand Oaks, CA


