Regulatory Writing Senior Manager
Job description
About the Position
Regulatory Writing Senior Manager
United States - Remote
JOB ID: R-258566
LOCATION: United States - Remote
WORK LOCATION TYPE: Remote
DATE POSTED: Oct. 16, 2026
CATEGORY: Regulatory
SALARY RANGE: 139,581.90 USD - 188,846.10 USD
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you’re part of something bigger, it’s because you are. 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. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.
Responsibilities
- Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and Pediatric Investigation Plans
- Conduct the formal review and approval of authored documents, following applicable standard operating procedures
- With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
- Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
- Provide functional area input for Global Regulatory Plan and team goals
- Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
- Lead departmental and cross-departmental initiatives, as appropriate
- Generate document timelines
Requirements
Basic Qualifications:
- Doctorate degree and 2 years of directly related experience
- Master’s degree and 6 years of directly related experience
- Bachelor’s degree and 8 years of directly related experience
- Associate’s degree and 10 years of directly related experience
- High school diploma / GED and 12 years of directly related experience
Preferred Qualifications:
- Experience with regulatory documents in Regulatory Affairs, Research, Development or related area
- 5+ years of experience in medical writing in the Biotech/Pharmaceutical industry
We Offer
- 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
About the Company
At Amgen, we are relentless in applying the highest ethical standards to our products, services, and communications. We expect all job applicants to act with honesty and integrity. Providing any false or misleading information, or omitting material information during the hiring process, may result in immediate disqualification from the hiring process or termination if already employed. We appreciate your cooperation in helping us uphold these standards.
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.
Apply now for a career that defies imagination
Objects in your future are closer than they appear. Join us.
Attention Job Applicants: At Amgen, we are relentless in applying the highest ethical standards to our products, services, and communications. Consistent with this, we expect all job applicants to act with honesty and integrity. Providing any false or misleading information, or omitting material information during the hiring process, may result in immediate disqualification from the hiring process or termination if already employed. We appreciate your cooperation in helping us uphold these standards.
© Amgen. This job description was sourced from the employer's public career page. TheJob is not the employer — we index the posting and route candidates to the source. All content rights and hiring decisions belong to the employer.
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