Jobs and Careers
AM

Global Pharmacovigilance (PV) Scientist

Amgen
Thousand Oaks, United StatesRemotefull_timeVerifiedPosted 21 Apr 2025
💰 $122,105/yr

About the role

Career Category

Safety

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.

Global Pharmacovigilance (PV) Scientist

What you will do

Let’s do this. Let’s change the world. In this vital role you will work with the Therapeutic Safety Teams for safety assessment activities for medical/scientific operations. This person will also provide scientific and compliance expertise as needed to GPS.

Responsibilities

  • Contribute to the planning, preparation, writing and review of non-medical portions of aggregate reports

  • Collaborate with affiliates and other internal Amgen partners regarding deliverables

  • Review of AE/SAEs from clinical trials as needed

  • Review and provide input and support on study protocols, statistical analysis plans and other clinical study-related documents

  • Review standard design of tables, figures, and listings for safety data from clinical studies

  • Participate in development of safety-related data collection forms for clinical studies

  • Attend study team meetings as requested or needed

  • Conduct signal detection, evaluation, and management

  • Perform data analysis to evaluate safety signals and write up analysis results in collaboration with GSO

  • Prepare safety assessment reports and other safety documents and regulatory responses

  • Search and review adverse event data, literature, and other safety-relevant data for the purpose of signal detection

  • Participates in Safety Governance per Amgen processes

  • Prepare presentation of the Global Safety Team’s recommendations on safety issues to the cross-functional decision-making body

  • Assist GSOs and other Senior Scientists in the development of risk management strategy and activities

  • Provides contents for risk management plans

  • Update strategy and content for regional risk management plans

  • Assist GSOs to oversee risk minimization activities including tracking of activities as needed

  • Evaluate risk minimization activity

  • Prepare response to regulatory inquiries related to risk management plans under the guidance of GSO

  • Support activities related to new drug applications and other regulatory filings

  • Assist GSO/ or other Senior Scientist in developing a strategy for safety-related regulatory activities

  • Provide safety contents for filings

  • Performs other duties related to the position as necessary as defined in Standard Operating Procedures or as requested by supervisor

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 scientist with these qualifications.

Basic Qualifications:

  • Doctorate degree OR

  • Master’s degree and 2 years of relevant experience OR

  • Bachelor’s degree and 4 years of relevant experience

Preferred Qualifications:

  • RN, PharmD, MPH or PA

  • Minimum 3 years direct experience in pharmacovigilance: signal detection and evaluation; data analysis interpretation and synthesis; periodic report production

  • Knowledge of processes and regulations for pharmacovigilance and risk management

  • Clinical/medical research experience

What you can expect from 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 Ric

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Amgen

View company profile →