Global Safety Medical Director (GSO) - Hematology/Oncology, US- Remote
AmgenUs - pennsylvania - philadelphiaUpdate time: November 19,2021
Job Description

Career Category

Safety

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

Global Safety Medical Director - Hematology/Oncology

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will be accountable for the staff management and resource allocations in Global Patient Safety and support GPS in the establishment of a highly effective global safety organization in full compliance to worldwide regulations.

The Global Safety Officer (GSO) serves 2 roles:

  • Safety expert of the assigned product(s), establishing the strategy, direction, and priorities of pharmacovigilance activities. The GSO is accountable for the overall safety profile and all product-related decisions and deliverables for assigned products supporting Hematology-Oncology portfolio.
  • The GSO leads the Safety Analysis Team (SAT), Global Safety Team (GST) and is a core member of the Executive Safety Committee (ESC). The GSO also is a member of the Evidence Generation Team and other relevant cross functional teams. The GSO will be assigned as delegate for the TAH as needed.

Key activities

  • Validate safety signals and lead safety signal assessments
  • Develop and maintain Core Safety Information (core data sheet, core risks in informed consent forms, etc.)
  • Prepare/review core and regional risk management plans including additional risk minimization measures
  • Prepare/review safety sections of periodic aggregate reports
  • Provide safety input to protocols, statistical analysis plans, and clinical study reports
  • Prepare/review safety sections of new drug applications and other regulatory filings
  • Serve as safety expert on Evidence Generation Team for assigned products
  • Inspection Readiness

Win

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 with these qualifications.

Basic Qualifications

  • MD or DO degree from an accredited medical school
  • 4 or more years of industry pharmacovigilance (PV) experience

AND

  • Completion of an accredited medical or surgical residency

Or

  • Clinical experience in either an accredited academic setting or private practice (including hospital based) setting.

Preferred Qualifications

  • Product safety in the bio/pharmaceutical industry or regulatory agency
  • Previous management and/or mentoring experience
  • Experience in the study/research and/or treatment of Hematology and Oncology disease states

Thrive

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Apply now

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

Amgen will consider for employment qualified applicants with criminal histories in a manner consistent with the San Francisco Fair Chance Ordinance.

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