Remote Senior Medical Director - Hematology/Oncology

IQVIA Argentina

Durham (NC)

On-site

USD 186,000 - 519,000

Full time

14 days+
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Job summary

IQVIA seeks a Senior Medical Director in Hematology/Oncology, home-based in the U.S. or Canada, to provide strategic medical leadership across global clinical research programs and serve as Medical Monitor.

You will oversee protocol interpretation, safety review, and medical data review while collaborating with sponsors, investigators, and internal teams to ensure compliant, efficient trials. This role emphasizes medical oversight, data interpretation, and strategic input for study design and

Qualifications

  • MD degree from an accredited medical school.
  • 5–7+ years of clinical experience as a licensed physician in Oncology/Hematology or related fields.
  • Board certification or eligibility in the relevant therapeutic area preferred.
  • ≥3 years of clinical research experience as a study physician/investigator or in Pharma/CRO/Biotech environments.

Responsibilities

  • Provide medical and scientific input to global clinical research programs, including data review and safety evaluation.
  • Oversee medical monitoring plans and act as primary medical resource for study teams and sites.
  • Ensure compliance with GCP and maintain high efficiency of medical activities.
  • Support site selection, investigator engagement, and patient recruitment strategies.
  • Review safety data (SAEs, etc.) and manage unblinding procedures when required.

Skills

MD
Clinical leadership
Medical monitoring
Global trial expertise

Education

MD from an accredited medical school

Job description

IQVIA seeks a Senior Medical Director in Hematology/Oncology, home-based in the U.S. or Canada, to provide strategic medical leadership across global clinical research programs and serve as Medical Monitor.

You will oversee protocol interpretation, safety review, and medical data review while collaborating with sponsors, investigators, and internal teams to ensure compliant, efficient trials. This role emphasizes medical oversight, data interpretation, and strategic input for study design and

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