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Medical Review Scientist

Job in Oxnard, Ventura County, California, 93030, USA
Listing for: Randstad Life Sciences US
Full Time position
Listed on 2026-09-22
Job specializations:
  • Healthcare
    Medical Science
Salary/Wage Range or Industry Benchmark: 60 - 69.09 USD Hourly USD 60.00 69.09 HOUR
Job Description & How to Apply Below

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Job Summary

As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health.

With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!



Job Summary

As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health.

With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!

Key Skills

  • Nursing degree needed
Drug Safety

Pharmacovigilance

Medical review/ Safety Review

location:
Telecommute

job type:
Contract

salary: $60.00 - 69.09 per hour

work hours: 9 to 5

education:
Bachelors

Responsibilities

Responsibilities
  • Execute 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 as assigned
  • Execute ICSR case escalation as appropriate
  • Execute 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
  • Support Quality Assurance of ICSR medical review
  • Participate in Safety Assessment Team (SAT) (if applicable)
  • Conduct reportability assessment for medical device associated events and /or product complaint associated events, and review for potential product problems
  • Provide input on teams for interdepartmental and cross-functional initiatives (if applicable)
  • Perform other duties related to the position as necessary as defined in SOPs or as requested by his/her 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
Qualifications

Required:

  • Clinical Nursing qualification + 1 year drug safety experience.
  • Nursing Degree + 3 years relevant work experience.
  • Medical review of ICSRs (narratives, coding, expectedness, causality, seriousness).
  • Quality Assurance of ICSR medical review.
  • Clinical knowledge of therapeutic area patient populations and drug class.
skills:
Quality Assurance, ICSR (Individual Case Study Report), QC Review

Equal Opportunity

Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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