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Global Regulatory Writing Manager

10-12 years
Not Disclosed
10 Dec. 3, 2024
Job Description
Job Type: Full Time Education: PhD/BSc/MSc/DPharma/PharmD/MBBS/BDS/BAMS/BHMS/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Medical Writer – Regulatory Submissions
Location: Flexible (Remote and On-Site Opportunities Available)
Employment Type: Full-Time


About Amgen

For over 40 years, Amgen has been at the forefront of biotechnology, using cutting-edge science and data to discover, develop, manufacture, and deliver medicines that make a real difference in the lives of millions of patients. Our commitment to innovation and excellence has driven breakthroughs in oncology, inflammation, general medicine, and rare diseases. Now is your chance to join our team and help transform healthcare worldwide.


What You Will Do

Let’s do this. Let’s change the world.

As a Medical Writer, you’ll play a vital role in developing and delivering regulatory and scientific submission documents. Collaborating across teams, you will ensure compliance with global regulatory standards while supporting Amgen’s mission to provide innovative treatments for patients.

Key Responsibilities:

  • Document Creation:
    Author and secure approval for regulatory submission documents, including Clinical Study Reports, Investigator Brochures, Protocols, Briefing Documents, Pediatric Investigation Plans, and more.

  • Review and Approval:
    Conduct thorough reviews of documents, ensuring adherence to applicable standard operating procedures (SOPs).

  • Project Leadership:
    Manage regulatory writing activities for submissions, including drug applications and biologics license applications.

  • Functional Team Leadership:
    Act as a functional area lead on key teams such as the Global Regulatory Team, Evidence Generation Team, or Label Working Group.

  • Collaboration:
    Work with contract and freelance writers as necessary, providing functional input for global regulatory plans and team goals.

  • Training and Mentorship:
    Train and mentor junior writers, contributing to their professional growth.

  • Timelines and Planning:
    Develop and manage timelines for document completion, ensuring alignment with team goals.

  • Continuous Learning:
    Stay current with advancements in technology and industry regulations to ensure compliance and innovation.


What We Expect of You

We value diversity and the unique contributions of each team member. For this role, we seek an experienced professional with the following qualifications:

Basic Qualifications:

  • Doctorate degree OR
  • Master’s degree and 4-6 years of directly related experience OR
  • Bachelor’s degree and 6-8 years of directly related experience OR
  • Diploma and 10-12 years of directly related experience

Preferred Qualifications:

Technical Skills:

  • Proficiency with Microsoft Office tools
  • Deep knowledge of scientific and technical writing, editing, and the clinical development process
  • Familiarity with International Council on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines

Soft Skills:

  • Strong written and verbal communication
  • Proven leadership, collaboration, and problem-solving abilities
  • Excellent time management and attention to detail
  • Self-motivated with a commitment to delivering results

What You Can Expect of Us

At Amgen, we’re not just developing medicines—we’re building careers. From our competitive salaries to our comprehensive benefits, we are dedicated to your growth and well-being.

Benefits Include:

  • Comprehensive health and wellness plans
  • Retirement savings plans with company contributions
  • Paid time off and company-wide shutdowns
  • Flexible work arrangements
  • Career development opportunities and mentorship programs

Apply Now

Join us for a career that defies imagination. Transform lives, including your own, by becoming part of Amgen’s mission-driven team.

Visit careers.amgen.com to apply.


Amgen is an Equal Opportunity Employer, committed to diversity and inclusion. We welcome applicants from all backgrounds and provide accommodations for individuals with disabilities throughout the hiring process.