Senior Medical Director, Hematology/Oncology

Senior Medical Director, Hematology/Oncology Home-based in the U.S. or Canada 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. Clinical Leadership & Study Execution Support 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 and collaborate with sponsors and internal safety teams Manage unblinding procedures when required and contribute to regulatory interactions as needed Data Review & Reporting Provide medical review of clinical data, including eCRFs, tables, and listings, to ensure accuracy and consistency Contribute to data interpretation and support development of clinical study reports Business Development & Strategy Support Support proposal development, feasibility assessments, and client presentations Provide medical expertise to strengthen study design and strategic positioning in new business opportunities Additional Contributions Support development of internal processes, training, and quality improvement initiatives Contribute to scientific literature review and medical input across projects as needed Qualifications & Experience 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) Board certification or eligibility in the relevant therapeutic area strongly preferred Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environments Key Competencies Strong ability to collaborate effectively within multidisciplinary and matrixed global teams, driving alignment and consensus Demonstrated 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 The potential base pay range for this role, when annualized, is $186,300.00 - $519,000.00. Incentive plans, bonuses, and/or other forms of compensation may be offered, alongside a range of health and welfare benefits. EEO Statement IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by applicable law. IQVIA maintains a zero tolerance policy for candidate fraud. #J-18808-Ljbffr