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Principal Scientist - Clinical Pharmacology, Modeling & Simulation
Principal Scientist - Clinical Pharmacology, Modeling & SimulationAmgen • South San Francisco, CA, United States
Principal Scientist - Clinical Pharmacology, Modeling & Simulation

Principal Scientist - Clinical Pharmacology, Modeling & Simulation

Amgen • South San Francisco, CA, United States
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.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.

Principal Scientist - Clinical Pharmacology, Modeling & Simulation

What you will do

Let's do this. Let's change the world. The Clinical Pharmacology, Modeling & Simulation Department at Amgen is seeking a Principal Scientist. In this vital role, you will drive innovative modeling and simulation strategies for translational approaches to support clinical dosage selections and clinical study designs. Your impact will extend across therapeutic areas such as oncology, rare diseases, obesity, and cardiovascular disease, and spans diverse modalities from small molecules and mAbs to innovative novel modalities.

The Principal Scientist will be Subject Matter Expert who will apply Quantitative Translational and Clinical Pharmacology approaches - such as Pharmacokinetic/Pharmacodynamic (PK/PD) modeling, Mechanistic-Physiologically Based Pharmacokinetic (M-PBPK) modeling, Mechanistic-PBPK-Pharmacodynamic (M-PBPK-PD) modeling, Quantitative Systems Pharmacology (QSP) modeling - integrated with emerging Machine Learning and Generative AI approaches - to innovatively guide optimal clinical drug development.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications:

Doctorate degree and 2 years of Clinical Pharmacology and Modeling & Simulation experience

Or

Master's degree and 4 years of Clinical Pharmacology and Modeling & Simulation experience

Or

Bachelor's degree and 6 years of Clinical Pharmacology and Modeling & Simulation experience

Or

Associate's degree and 10 years of Clinical Pharmacology and Modeling & Simulation experience

Or

High school diploma / GED and 12 years of Clinical Pharmacology and Modeling & Simulation experience

Preferred Qualifications:

  • PhD (in Pharmacokinetics or Pharmaceutical Sciences or Pharmacology or Chemical Engineering or equivalent professional degrees e.g. MD, PharmD).

  • 5+ years of experience in Clinical Pharmacology, Modeling & Simulation in the Biotechnology/Pharmaceutical Industry.

  • Hands-on experience in Quantitative Clinical Pharmacology approaches with a focus on PK/PD modeling, M-PBPK modeling, M-PBPK-PD modeling, and QSP modeling to inform clinical study designs, optimal dosage selection in target patient populations, characterization of drug-drug interactions, dosing in special populations, ethnic sensitivity, pediatric and biopharmaceutics studies. Expert knowledge of commonly used software for PK/PD, M-PBPK, M-PBPK-PD, & QSP modeling required.

  • Established track-record of Model Based Drug Development (MIDD).

  • Established track-record of interaction with global health authorities, authoring regulatory documents, knowledge of global regulatory requirements and guidance.

  • Experience in leading the design and implementation of clinical pharmacology and biopharmaceutic studies including bioequivalence, bio-comparability, drug-drug interaction, special population, ethnic sensitivity, ADME and pediatric studies and integrating results into regulatory filings, and product labels.

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

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.

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.

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Principal Scientist - Clinical Pharmacology, Modeling & Simulation • South San Francisco, CA, United States

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