Job Posting Title- Senior Medical Director, Hematology/OncologyLocation: Home-based in the U.S. or CanadaJob OverviewThe 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.Essential FunctionsProvides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation and reportingEnsures medical activities run according to GCP and operate with highest efficiencyEstablishes and maintains a network of medical/scientific consultants, etc.Clinical Leadership & Study ExecutionSupport site selection, investigator engagement, and patient recruitment/retention strategiesTrain study teams and investigators on protocol and therapeutic areaDevelop and oversee medical monitoring plans and serve as the primary medical resource for study teams and sitesSafety & Medical OversightEnsure medical oversight of patient safety, including ongoing assessment of the study safety profileReview and interpret safety data, including SAEs and critical clinical data, ensuring accuracy and appropriate follow-upSupport safety reporting activities and collaborate with sponsors and internal safety teamsManage unblinding procedures when required and contribute to regulatory interactions as neededData Review & ReportingProvide medical review of clinical data, including eCRFs, tables, and listings, to ensure accuracy and consistencyContribute to data interpretation and support development of clinical study reportsBusiness Development & StrategySupport proposal development, feasibility assessments, and client presentationsProvide medical expertise to strengthen study design and strategic positioning in new business opportunitiesAdditional ContributionsSupport development of internal processes, training, and quality improvement initiativesContribute to scientific literature review and medical input across projects as neededQualifications & ExperienceMD from an accredited, internationally recognized medical school5–7+ 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 or equivalent experience.Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environmentsKey CompetenciesStrong ability to collaborate effectively within multidisciplinary and matrixed global teams, driving alignment and consensusDemonstrated ability to work independently while managing multiple priorities in a dynamic environmentExcellent organizational skills with the ability to manage complex projects with shifting timelines and requirementsExceptional communication and interpersonal skills, with the ability to translate complex medical concepts into clear, actionable insights#LI-Remote#LI-NITINMAHAJANIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA 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, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $186,300.00 - $519,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.