Medical Director – Oncology

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🔥 0 minutes ago

🌐 Turkey, Portugal, +3 more countries – Remote

🇹🇷 Turkey – Remote 🇵🇹 Portugal – Remote 🇭🇺 Hungary – Remote 🇬🇷 Greece – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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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 medical and scientific input to clinical research programs, including review of proposals, clinical data, protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plans, study reports, regulatory submissions, and adverse event evaluations • Ensure medical activities comply with GCP and operate efficiently • Serve as Medical Monitor and primary medical contact for sponsor medical teams, investigators, site coordinators, and project teams • Interact with clients, sponsor representatives, investigators, key opinion leaders, and multidisciplinary project teams on drug development, study design, protocols, endpoints, and eligibility criteria • Provide protocol and therapeutic-area training and present protocol or safety information at investigator meetings • Support investigator site selection, subject recruitment and retention, and investigator/site communications • Develop medical monitoring plans and provide on-call coverage for protocol queries and site medical support • Monitor patient safety, review SAE reports and narratives, track safety queries, and support safety reporting and regulatory interactions • Review eCRFs, data analysis plans, safety fields, medical coding, data tables, listings, figures, and clinical study reports • Support DSMB/adjudication committee activities and ensure feedback reaches sites • Support business development through proposal development, marketing presentations, sales presentations, and feasibility discussions • Conduct literature searches, prepare training sessions, interpret clinical data, draft procedures, and participate in quality improvement efforts • Perform other related duties assigned or requested by the Chief Medical Officer

🎯 Requirements

• Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education • 10 years of experience required, including medical practice, academia, clinical research, or drug development • 3–5 years of biopharmaceutical industry experience preferred, which may be part of the 10-year experience • Oncology/Hematology Board Certified or Board Eligible in Oncology required • Preferably a Urologist or Surgical Oncology specialist • Ability to work with multidisciplinary colleagues and translate concepts into practical approaches • Ability to work independently with minimal supervision and effectively within a team and matrix environment • Ability to organize and work efficiently across several projects with shifting priorities • Excellent oral and written communication and interpersonal skills • Commitment to truthful and complete application information and credentials