Senior Medical Director, Hematology/Oncology

🔥 1 minute ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Provide scientific, clinical, and operational oversight across global clinical research programs • Act as Medical Monitor and primary medical interface between IQVIA, sponsors, and investigative sites • Guide protocol interpretation, eligibility, compliance, safety, medical data review, and responses to urgent medical queries • Provide medical and scientific input on business proposals, clinical data, protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plans, clinical study reports, regulatory submissions, and adverse events • Ensure medical activities follow GCP and operate efficiently • Establish and maintain a network of medical and scientific consultants • Support site selection, investigator engagement, and patient recruitment and retention strategies • Train study teams and investigators on protocols and therapeutic areas • Develop and oversee medical monitoring plans • Oversee patient safety and assess study safety profiles • Review and interpret safety data, including SAEs and critical clinical data • Support safety reporting and collaborate with sponsors and internal safety teams • Manage unblinding procedures and contribute to regulatory interactions • Review clinical data, including eCRFs, tables, and listings • Contribute to data interpretation and clinical study reports • Support proposal development, feasibility assessments, and client presentations • Provide medical expertise for study design and new business opportunities • Support internal processes, training, and quality improvement initiatives • Contribute to scientific literature reviews and medical input across projects

🎯 Requirements

• MD from an accredited, internationally recognized medical school • 5–7+ years of clinical experience as a licensed physician within Oncology, Hematology, Surgical Oncology, or Urology with oncologic focus • Board certification or eligibility in the relevant therapeutic area strongly preferred or equivalent experience • Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environments • Advanced English level, able to speak and communicate fluently • Strong ability to collaborate effectively within multidisciplinary and matrixed global teams • Ability to work independently while managing multiple priorities in a dynamic environment • Excellent organizational skills with the ability to manage complex projects with shifting timelines and requirements • Exceptional communication and interpersonal skills, with the ability to translate complex medical concepts into clear, actionable insights

🏖️ Benefits

• Global scope and collaboration with global teams • Opportunities to contribute to internal processes, training, and quality improvement initiatives