Regulatory Writing Senior Manager

Amgen; United States; Remote; USD 140,000 - 189,000; Full time

Job summary

Amgen is seeking a Regulatory Writing Senior Manager to lead writing activities for complex product submissions in a remote United States setting. You will supervise contract writers, mentor junior writers, and serve as a functional area lead on cross-functional teams to ensure timely, compliant documentation for regulatory submissions.

You will drive timelines, contribute to Global Regulatory Plans, and oversee high-quality deliverables across Clinical Study Reports, IBs, and eCTD modules,

Qualifications

• Doctorate, Master’s, or Bachelor’s degree in a related field.
• Significant regulatory writing experience in biotech/pharma.
• Leadership and mentoring of junior writers required.

Responsibilities

• Authors/regulatory submission documents for complex products.
• Review and approve drafted documents per SOPs.
• Lead writing activities for new/supplemental submissions (eCTD).
• Supervise contract/freelance writers and mentor juniors.
• Lead departmental initiatives and generate document timelines.

Skills

Regulatory writing

Leadership

Mentoring

Education

Doctorate degree

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Job description

Regulatory Writing Senior Manager### Regulatory Writing Senior ManagerApply: Remote: United States - Remote: Full time: Posted Today: R-258566## **Career Category**Regulatory## ## **Job Description****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.## Regulatory Writing Senior Manager## **Live****What you will do**Let’s do this. Let’s change the world. In this key role you will serve as the functional area lead on product teams, lead writing activities for complex product submissions, provide functional area expertise, train and mentor more junior writers, and lead departmental activities. Key responsibilities include:* 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## **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 leader with these qualifications.## **Basic Qualifications:**Doctorate degree and 2 years of directly related experienceORMaster’s degree and 6 years of directly related experienceORBachelor’s degree and 8 years of directly related experienceORAssociate’s degree and 10 years of directly related experience## OrHigh 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## **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.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 deadlineAmgen 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**139,581.90USD -188,846.10 USD