IQVIA

life sciences and healthcare

SeniorMedicalDirector,Hematology/Oncology

$186–519k Durham, North Carolina, United States; United States; Canada FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Medical Director, Hematology/Oncology at IQVIA. Skills: Hematology/Oncology, Clinical Research, Medical Oversight. Provide medical and scientific input to clinical research programs. Ensure medical activities run according to GCP”

Industry & Context.

life sciences and healthcare

What They're Looking For.

Must Have

MD from an accredited, internationally recognized medical school, 5–7+ years of clinical experience as a licensed physician within the relevant specialty (Oncology, Hematology, Surgical Oncology, or Urology with oncologic focus), Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environments

Nice to Have

Board certification or eligibility in the relevant therapeutic area

What You'll Do.

Provide medical and scientific input to clinical research programs

Ensure medical activities run according to GCP

Establish and maintain a network of medical/scientific consultants

Support site selection

investigator engagement

and patient recruitment/retention strategies

Train study teams and investigators on protocol and therapeutic area

Develop and oversee medical monitoring plans

Serve as the primary medical resource for study teams and sites

Ensure medical oversight of patient safety

Review and interpret safety data

Support safety reporting activities

Manage unblinding procedures when required

Contribute to regulatory interactions as needed

Provide medical review of clinical data

Contribute to data interpretation

Support development of clinical study reports

Support proposal development

feasibility assessments

and client presentations

Provide medical expertise to strengthen study design

Support development of internal processes

and quality improvement initiatives

Contribute to scientific literature review and medical input across projects

How You'll Work.

Team & Collaboration

Collaborate effectively within multidisciplinary and matrixed global teams; Driving alignment and consensus

Communication Scope

Exceptional communication and interpersonal skills; Translate complex medical concepts into clear, actionable insights

Process & Methodology

Manage multiple priorities in a dynamic environment, Manage complex projects with shifting timelines and requirements

Full Job Description

**Job Posting Title- Senior Medical Director, Hematology/Oncology** **Location: Home-based in the U.S. or Canada** **Job Overview** The Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and operational oversight across global clinical research programs. Acting as Medical Monitor, this role serves as the primary medical interface between IQVIA, sponsors, and investigative sites—ensuring high-quality, compliant, and efficient trial execution. The role provides hands-on medical oversight, guiding protocol interpretation, eligibility, compliance, and safety, including medical data review and review of critical clinical data (e.g., alert laboratory results) and timely response to urgent medical queries to ensure patient safety and study continuity. **Essential Functions** * Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation and reporting * Ensures medical activities run according to GCP and operate with highest efficiency * Establishes and maintains a network of medical/scientific consultants, etc. **Clinical Leadership & Study Execution** * Support site selection, investigator engagement, and patient recruitment/retention strategies * Train study teams and investigators on protocol and therapeutic area * Develop and oversee medical monitoring plans and serve as the primary medical resource for study teams and sites Safety & Medical Oversight * Ensure medical oversight of patient safety, including ongoing assessment of the study safety profile * Review and interpret safety data, including SAEs and critical clinical data, ensuring accuracy and appropriate follow-up * Support safety reporting activities

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