
Healthcare Insurance • Biotechnology • Artificial Intelligence
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.
10,000+ employees
⚕️ Healthcare Insurance
🧬 Biotechnology
🤖 Artificial Intelligence
💰 $1G Post-IPO Debt on 2023-05
September 18

Healthcare Insurance • Biotechnology • Artificial Intelligence
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.
10,000+ employees
⚕️ Healthcare Insurance
🧬 Biotechnology
🤖 Artificial Intelligence
💰 $1G Post-IPO Debt on 2023-05
• Provide medical and scientific support to clinical research programs, study teams and investigators. • Serve as Medical Monitor and provide medical oversight for clinical trials conducted by IQVIA Biotech Clinical on behalf of sponsors. • Be available to answer site coordinators and investigators 24/7 for protocol inclusion/exclusion questions, clarifications, and compliance issues. • Review and provide medical input on study protocols, informed consent, Investigator Brochures, eCRFs, analysis plans, and clinical study reports. • Ensure medical activities run according to GCP and maintain highest efficiency; supervise/manage Medical Director activities. • Interact with clients, thought leaders, and sponsor representatives on drug development programs, study design, investigator selection, and endpoints. • Develop and deliver project team training and assist with subject recruitment and retention activities. • Provide safety monitoring: medical review of SAE reporting, SAE narratives, IND/SUSAR reports, Investigator Brochure updates, and annual IND reports. • Perform medical review of eCRFs, data analysis plans, medical coding, data reconciliation, and review of tables/listings/figures. • Participate in DSMB/Adjudication Committee activities, convene proceedings, and develop operating guidelines as needed. • Support business development with proposal development, sales presentations, and feasibility discussions. • Conduct literature searches, prepare training sessions, assist with SOPs, and participate in quality improvement and special projects.
• Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. • Minimum 10 years of experience (can include medical practice, academia, clinical research, or drug development). • 3-5 years of biopharmaceutical (industry) experience preferred (may be part of the 10-year experience). • Current or prior license to practice medicine; board certification/eligibility ideal. • Board Certified / Board Eligible: Hematology (Required). • Applicants must have experience in at least one: Hematology (Non-Malignant), Hematological Malignancies, Pediatric Hematology, or Adult Hematology. • Ability to work in partnership with a multidisciplinary group and promote consensus. • Outstanding ability to work independently with minimal supervision and within a team/matrix environment. • Ability to organize and work efficiently on several projects with shifting priorities. • Excellent oral and written communication and interpersonal skills.
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