<h2>Career Category</h2>Clinical<h2></h2><h2>Job Description</h2>Join Amgen’s Mission of Serving PatientsAt 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.Supplier Governance ManagerWhat you will doLet’s do this. Let’s change the world. In this vital role you will maximize the value obtained from partnerships with external providers across the R&amp;D organization and ensure appropriate financial oversight of Clinical Trial suppliers.Responsibilities<ul><li>Lead team responsible for managing study level Purchase Orders (POs) work orders and budgets with clinical service providers e.g. CROs, Labs etc</li><li>Ensure quality of Purchase Orders (POs) including SoW negotiations, funding requests through established financial processes, PO execution, ongoing budget review, and PO closure</li><li>Work with suppliers and internal customers (typically up to Director level) to identify, manage, escalate and resolve issues related to study level PO approvals, invoice issues etc.</li><li>Develop and maintain functional processes and ensure team adherence to them.</li><li>Communicate Amgens financial, PO and invoice management standards across suppliers and Amgen teams. Support suppliers to meet Amgens requirements as needed.</li><li>Serve as R&amp;D SME (subject matter expert) for work orders, POs, invoicing and associated systems e.g. ERP system, TMF system.</li><li>Liaise cross functionally e.g. with finance, procurement and business counterparts to support clinical trial budgeting and accounting in relation to clinical trial suppliers.</li><li>Provide ongoing supplier oversight and encourage sharing of standard methodologies and development of process improvements</li><li>Chairing and leading supplier governance meetings</li></ul>What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is proficient with these qualifications.Basic Qualifications:<ul><li>Doctorate degree OR</li><li>Master’s degree &amp; 2 years of clinical development, discovery research or translational science experience OR</li><li>Bachelor’s degree &amp; 4 years of clinical development, discovery research or translational science experience OR</li><li>Associate’s degree &amp; 8 years of clinical development, discovery research or translational science experience OR</li><li>High school diploma / GED &amp; 10 years of clinical development, discovery research or translational science experience</li></ul>Preferred Qualifications:<ul><li>BA/BS/BSc in the sciences or RN</li><li>Proven work experience in life sciences or medically related field, including biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company), discovery research or translational science</li><li>Experience in clinical supplier contracting, work orders and budgets</li><li>Experience with global ERP systems, PO management, invoice management</li><li>Experience as team leader or line manager</li><li>Experience working at or with, clinical research suppliers (CROs, central labs, imaging suppliers etc.</li><li>Experience working in a global, matrix organization</li><li>Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines and international regulatory requirements/guidelines</li><li>Strong problem solving skills and critical thinking to effectively identify solutions</li><li>Support business functions with selection and development of new suppliers</li><li>Ensure adherence to standard methodologies by Amgen functional areas</li><li>Collaborate closely with functional areas across the R&amp;D organization to ensure internal business needs are being met</li><li>Contribute to, and as appropriate, lead departmental and cross-functional initiatives and special projects as identified by management or business need</li></ul>What you can expect from usAs 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:<ul><li>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</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models, including remote and hybrid work arrangements, where possible</li></ul>Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn 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.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.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. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status..Salary Range104,833.00 USD - 129,025.00 USD