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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 biotech in our fight against the world’s toughest diseases. With a focus on 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 lives.
Our award-winning culture is collaborative, innovative, and science-based. If you have a passion for challenges and the opportunities that lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
What You Will Do
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 the 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. 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 Masters degree and 4 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field Bachelors degree and 6 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field Associates 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 What You Can Expect From Us
We support 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 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 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. For more information, visit careers.amgen.com. Equal Opportunity
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 provide 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. In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
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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 the 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. 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 Masters degree and 4 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field Bachelors degree and 6 years of medical writing in Biotechnology, Pharmaceutical, or another Healthcare-related field Associates 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 What You Can Expect From Us
We support 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 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 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. For more information, visit careers.amgen.com. Equal Opportunity
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 provide 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. In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
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