HEOR Value Writing, Senior Manager

Career Category

Health Economics

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.

HEOR Value Writing, Senior Manager

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will transform the lives of patients through.

• Prepares, edits, and finalizes key HEOR documents such as Global Value Dossiers, Briefing Books for early HTA advice, AMCP dossiers, EU Joint Clinical Assessment dossiers – in close collaboration with the HEOR Product Lead and cross-functional team.
• Provides writing support for study protocols, synopses, abstracts, posters, presentations, and manuscripts.
• Collaborates with clinicians, clinical scientists, biostatisticians, etc. to ensure study results and statistical interpretations are accurately and clearly reflected in the relevant HEOR documents.
• Is a proficient user of AI authoring tools for drafting, updating and finalizing HEOR documents.
• Identifies changes, modifications, and improvements to the document preparation processes and templates to improve quality, efficiency, and productivity.
• Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.
• Ensures that value writing deliverables conform to all relevant internal and external guidelines – depending on the specific deliverable.
• Creates and maintains standard operating procedures and work instructions for preparation and maintenance of compliant value writing deliverables.
• Supports development of training materials for onboarding new value writers; ensures consistent application of writing best practices.
• Ensures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in agreed document management system.
• Ensures that appropriate documented quality control (QC) checks are performed on value writing deliverables, responds to findings, and recommends quality process improvements.
• Reports to the Head of HTA Strategy & Project management, HEOR

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The medical writing professional we seek is research driven with these qualifications.

Basic Qualifications:

• Doctorate degree and 2 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field

• Master’s degree and 4 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field

• Bachelor’s degree and 6 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field

• Associate’s degree and 10 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field

• High school diploma / GED and 12 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field

Preferred Qualifications:

• Excellent English (native if possible) and very good writing and word processing skills
• Comfortable communicating with people from a range of backgrounds, internally and externally.
• Excellent attention to detail when preparing/editing documents as well as when reviewing clinical data
• Experience in working in cross-functional teams within a matrix organization.
• Experience using various word-processing/text editing/ reference management tools.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth an