FreshRemote.Work

Global Safety Sr Medical Scientist

US - California - Thousand Oaks - Field/Remote

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.

Global Safety Sr Medical Scientist

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will provide medical review of individual case safety reports (ICSRs) in support of safety surveillance for Amgen products and support global individual case safety reports regulatory reporting compliance.

  • Implement the medical review of ICSRs (narratives, coding, expectedness, causality and seriousness) to ensure quality reports. Produce medically accurate ICSRs reports
  • Act as MSRT product lead and/or therapeutic area lead as assigned
  • Complete ICSR case issue to GSO as appropriate
  • Implement appropriate case follow up per SOPs
  • Support medical coding conventions, and systematic process improvements for ICSR medical review
  • Maintain list of expected terms in the auto label tool
  • Monitor the compliance of autolabel tool updates
  • Support Quality Assurance of ICSR medical review
  • Act as MSRT process lead and support the development, training on and implementation of new processes in MSRT
  • Support training to Amgen employees on ICSR medical review
  • Mentor junior medical reviewers. As needed and applicable, provide direct managerial responsibilities for medical reviewers on their therapeutic or functional team
  • Participate in Safety Assessment Team (SAT)
  • Conduct reportability assessment for medical device associated events and/or product complaint associated events, and review for potential product problems.
  • Provide expertise and guidance on teams for interdepartmental and cross-functional initiatives including process improvement, standards development, Standard Operating Procedures (SOP)creation, and metrics with regards to medical review
  • Perform other duties related to the position as necessary as defined in SOPs or as requested by their supervisor

Inspection Readiness:

  • Undertake activities delegated by the QPPV as detailed in the PV System Master File and maintain a state of inspection readiness
  • Be representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility

Win

What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek is a Senior Medical Scientist with these qualifications.

Basic Qualifications:

Doctorate degree and 3 years of experience

OR

Master’s degree and 6 years of experience

OR

Bachelor’s degree and 8 years of experience

Preferred Qualifications:

  • MD/DO or international equivalent plus 3 years relevant work
  • Knowledge of case management and medical review SOPs and regulatory requirements for Pharmacovigilance
  • Clinical knowledge of therapeutic area patient populations and drug class
  • Proficiency in technical safety systems
  • Knowledge of safety data capture in clinical trials and in the post marketing environments
  • Knowledge of clinical trials and drug development
  • Knowledge of Amgen products and patient population

Thrive

What you can expect of us

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

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.

Amgen offers a Total Rewards Plan comprising 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 including:

  • 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 and bi-annual company-wide shutdowns
  • Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

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.

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.

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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Salary Range

236,082.00 USD - 270,425.00 USD Apply

Job Profile

Regions

North America

Countries

United States

Benefits/Perks

Annual bonus program Career development Career development opportunities Comprehensive employee benefits package Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Life and Disability insurance Retirement and Savings Plan Total Rewards Plan

Skills

Biotechnology Case Management Clinical knowledge Clinical trials Compliance Drug Development Marketing Medical Coding Medical review Pharmacovigilance Process Improvement Quality Assurance Regulatory Compliance Safety Assessment Sales SOPS Teams

Tasks
  • Act as MSRT process lead
  • Act as MSRT product lead or therapeutic area lead
  • Be representative and point of contact for Health Authority Inspection and Internal Process Audits
  • Complete ICSR case issue to GSO
  • Conduct reportability assessment for medical device associated events and product complaint associated events
  • Implement appropriate case follow-up per SOPs
  • Implement medical review of ICSRs (narratives, coding, expectedness, causality, and seriousness)
  • Inspection Readiness
  • Mentor junior medical reviewers
  • Monitor autolabel tool updates
  • Participate in Safety Assessment Team (SAT)
  • Perform other duties related to the position as necessary
  • Provide expertise and guidance on interdepartmental and cross-functional initiatives
  • Provide medical review of individual case safety reports (ICSRs)
  • Support medical coding conventions and systematic process improvements
  • Support Quality Assurance of ICSR medical review
  • Support training on ICSR medical review
  • Training
  • Undertake activities for inspection readiness
Experience

3 years

Education

Bachelor's DO Doctorate Doctorate degree Master's

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9