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Regulatory Writing Manager

2+ years
Not Disclosed
10 Oct. 7, 2024
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

What You Will Do

Let’s make a difference together. In this essential role, you will be responsible for authoring various regulatory submission documents, including but not limited to:

  • Clinical Study Reports
  • Investigator Brochures
  • Responses to Questions
  • Protocols and Protocol Amendments
  • Informed Consent Forms
  • Tables of All Studies
  • Clinical Overview Addenda
  • eCTD Module 2 Clinical Summary Documents
  • Briefing Documents
  • Pediatric Investigation Plans
  • Other regulatory documents as needed

You will conduct formal reviews and approvals of authored documents in accordance with our standard operating procedures. Under supervision, you will manage regulatory writing activities for product submissions, including new and supplemental drug applications/biologics license applications.

As a functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group), you may provide valuable input for the Global Regulatory Plan and team objectives. You might also collaborate with contract and freelance writers and participate in training and mentoring junior medical writers.

In addition, you will help generate document timelines with team input and stay informed about relevant professional information and technology.

What We Expect of You

We value individuality and unique contributions in our mission to serve patients. The ideal candidate for this role is someone with:

Basic Qualifications:

  • Doctorate degree, or
  • Master’s degree with 3 years of directly related experience, or
  • Bachelor’s degree with 5 years of directly related experience, or
  • Associate’s degree with 10 years of directly related experience, or
  • High school diploma/GED with 12 years of directly related experience.

Preferred Qualifications:

Functional Skills:

  • Proficiency in word processing and Microsoft Office programs.
  • Strong knowledge of scientific/technical writing and editing, along with a solid understanding of the clinical development process for new compounds.
  • Ability to interpret and adhere to complex standard operating procedures (SOPs), guidance documents, and work instructions.
  • Familiarity with principles, concepts, theories, and standards in the scientific/technical field.
  • Extensive knowledge of International Council on Harmonization (ICH) guidelines and Good Clinical Practice (GCP) requirements.

Soft Skills:

  • Excellent written and verbal communication skills with a keen attention to detail.
  • Proven leadership capabilities within a team environment, demonstrating negotiation, persuasion, collaboration, and analytical judgment.
  • Strong time management and project management skills.
  • Self-motivated with a commitment to achieving results.

What You Can Expect From Us

At Amgen, we’re dedicated to your professional and personal growth. From competitive benefits to a collaborative culture, we support your journey every step of the way. Our comprehensive Total Rewards Plans align with local industry standards, in addition to your base salary.

Apply Now

Embark on a career that defies imagination. The opportunities in your future are closer than they appear. Join us.

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