Medical Director

IQVIA is seeking a Medical Director to join our Medical Services team and provide medical, clinical, and scientific leadership across global and regional clinical research programs. In this role, you will serve as a key medical expert throughout the clinical trial lifecycle, partnering with project teams, investigators, and clients to support protocol execution, participant safety, and scientific excellence. In addition to medical monitoring responsibilities, you will contribute strategic medical insight to business development activities, proposal development, and study design, helping to shape innovative solutions for our clients. Responsibilities: Primarily serve as the Global and/or Regional Medical Advisor on assigned clinical research projects. Serves as Scientific Advisor and provides medical and scientific guidance to project teams, ensuring the highest standards of patient safety, protocol compliance, and scientific integrity. Act as a trusted medical expert for investigative sites and study teams, supporting protocol interpretation, inclusion/exclusion determinations, patient eligibility assessments, and safety-related matters. Review and provide medical input into study protocols, Investigational Brochures, Case Report Forms (CRFs), and other key study documentation. Deliver therapeutic area and indication-specific training to clinical project teams. Attend and present at Investigator Meetings, client meetings, and other study-related forums. Perform medical review and clarification of trial-related Adverse Events (AEs) and support Serious Adverse Event (SAE) assessment in collaboration with Pharmacovigilance teams. Contribute to Analysis of Similar Events (AOSE), adverse event coding reviews, and other medical safety evaluations as required. Review Clinical Study Reports (CSRs), patient narratives, and other clinical study deliverables. Provide timely medical support for protocol-related questions from investigative sites throughout the course of a study. Support the development of medically sound study delivery strategies for regional and global clinical trials. Partner with Business Development and operational teams to provide medical and scientific expertise during proposal development, feasibility assessments, and bid defense meetings. Advise on therapeutic landscapes, standard of care, patient recruitment strategies, investigator identification, and competitive market considerations. Participate in client presentations, strategic business development activities, and scientific discussions with external stakeholders. Maintain awareness of emerging scientific, clinical, and regulatory developments within relevant therapeutic areas. Maintain awareness of industry development and contribute to scientific publications as appropriate. Qualifications: Medical degree from an accredited and internationally recognized medical school. Current or previous license to practice medicine.