HEOR Value Writing Sr Manager

HEOR Value Writing Sr Manager
United States - Remote Apply NowJoin 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 Sr Manager
What you will do
Let’s do this. Let’s change the world. In this vital role the HEOR Value Writing Sr Manager has the following responsibilities:
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 support for writing 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.
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.
Suggests or identifies changes, modifications, and improvements to the document preparation processes and templates in order to improve quality, efficiency, and productivity.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a collaborative partner with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of medical writing experience
OR
Master’s degree and 4 years of medical writing experience
OR
Bachelor’s degree and 6 years of medical writing experience
OR
Associate’s degree and 10 years of medical writing experience
Or
High school diploma / GED and 12 years of medical writing experience
Preferred Qualifications:
5 years’ experience in medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field
An understanding of the drug development process
Broad experience managing the medical writing responsibilities associated with multiple studies at various stages
Excellent communication 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
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 and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of 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 that may include:
A 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
Flexible work models, including remote and hybrid work arrangements, where possible
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
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Application deadline
Amgen anticipates accepting applications until 6/12/25; however, we may continue accepting applications beyond this date if we do not receive a sufficient number of candidates.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
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.