Jobs › Companies › Amgen › Senior Director, Clinical Risk & Insights

Sobre esta vaga de Senior Director, Clinical Risk & Insights na Amgen

Amgen · Remoto · United States - Remote

Career Category

Clinical

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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer.  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.



Senior Director, Clinical Risk & Insights

What you will do

Let’s do this. Let’s change the world. In this vital role you will lead Clinical Risk & Insights as a capability focused on Root Cause Analysis (RCA), systemic investigation, and clinical execution risk intelligence. Ensure significant, complex, recurring, and cross-portfolio issues generate clear executive insight, informed decisions, and sustained improvement. Set the GDO wide RCA approach and integrate systemic learning with portfolio risk intelligence, and the strategic direction of Risk-Based Quality Management (RBQM).


Responsibilities:

  • Set RCA methodology, investigation standards, guidance, and capability materials; lead complex investigations and coach teams to identify systemic causes and prevent recurrence.
  • Own triage and executive escalation of significant, complex, recurring, and cross-portfolio clinical execution issues; prioritize and direct RCA support.
  • Provide clinical risk insight, systemic learning, trend reports, and decision briefs to Management Review, the Clinical Trial Compliance Committee (CTCC), and CPSO leadership forums.
  • Challenge superficial root causes and ineffective CAPAs; recommend CAPA effectiveness actions, control redesign, intervention, or senior sponsorship when systemic clinical execution risk is identified.
  • Sponsor cross-functional improvement when system or control failures extend beyond one study or function; influence sustained change and embed risk-informed execution.
  • Sponsor the RBQM strategy and maturity roadmap, connecting systemic learning and portfolio risk intelligence with prospective risk identification and future study execution.
  • Lead and develop the department; set strategy and priorities, manage resources, budget, talent, and external expertise, and build organizational RCA capability.
  • Build strong relationships across Global Clinical Compliance & Support, Study Delivery Teams (SDTs), CPSO, GDO, R&D Quality, global networks, and external partners; contribute to relevant governance and standards.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients.


Basic Qualifications:

  • Doctorate degree + 4 years directly related experience or
  • Master’s degree + 8 years directly related experience or
  • Bachelor’s degree + 10 years directly related experience
  • AND 4 years direct managerial and/or leadership experience

Preferred Qualifications:

  • M.D., D.O., PhD, PharmD, or Master’s degree.

  • 11 years of experience in life sciences or a medically related field, including 8 years in biopharmaceutical clinical research.

  • Experience managing direct reports, including management-level staff.

  • Clinical risk management or RBQM experience, including study risk assessments, mitigation strategies, Critical to Quality (CtQ) factors, Key Risk Indicators (KRIs), and Quality Tolerance Limits (QTLs).

  • Experience analyzing quality event, audit, inspection, and readiness trends; operational excellence, continuous improvement, or quality intelligence.

  • Experience with analytics, automation, or knowledge-management tools; budget, resource, and organizational capacity management.


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 where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

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.

Application deadline

Amgen 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.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

 

 

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Salary Range

204,431.80USD -276,584.20 USD
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Sobre a Amgen

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients arou

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