Medical Director – Oncology

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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 support to clinical research programs, study teams, and investigators • Provide medical oversight for clinical trials as Medical Monitor on behalf of sponsor companies • Serve as primary contact for sponsor medical teams and frontline medical resource for project teams • Answer site coordinator and investigator questions on protocol criteria, clarifications, and compliance issues, including 24/7 on-call availability • Review clinical research proposals, data, protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plans, clinical study reports, regulatory submissions, and safety reports • Ensure medical activities comply with GCP and operate efficiently • Interact with clients, key opinion leaders, investigators, site staff, sponsor representatives, and FDA officials regarding drug development and study issues • Review and contribute to protocol development, study endpoints, inclusion/exclusion criteria, investigator selection, recruitment, retention, training, and investigator meetings • Develop medical monitoring plans and provide protocol query and site support coverage • Review SAE reports and narratives, track safety queries, assess study safety profiles, and review IND/SUSAR reports and Investigator Brochures • Review eCRFs, data analysis plans, safety fields, medical coding, data tables, listings, figures, and clinical study reports • Support DSMB/adjudication committee activities as requested • Support business development, 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 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 can be part of the 10-year experience • Oncology/Hematology Board Certified or Board Eligible in Oncology required • Urologist/Surgical Oncology background preferably • Ability to work with multidisciplinary colleagues and translate concepts into practical approaches • Ability to work independently with minimal supervision and effectively within team and matrix environments • Ability to organize and work efficiently across several projects with shifting priorities • Excellent oral, written, and interpersonal communication skills

🏖️ Benefits

• Potential incentive plans, bonuses, and/or other forms of compensation may be offered • Health and welfare benefits may be offered