Medical Director – Oncology (Sponsor Dedicated, Home‑Based)

About the role

The Medical Director – Oncology will provide medical and scientific oversight for sponsor‑dedicated oncology clinical trials conducted by IQVIA Biotech Clinical. Working remotely, the Director acts as the primary medical monitor, supporting study teams, investigators, and sponsor representatives throughout the trial lifecycle.

Key responsibilities

• Serve as the 24/7 medical monitor for oncology studies, answering protocol, safety, and compliance queries from sites and investigators.
• Review and contribute to study documents including protocols, informed consent forms, Investigator Drug Brochures, eCRFs, analysis plans, and clinical study reports.
• Ensure all medical activities comply with Good Clinical Practice (GCP) and sponsor standards.
• Develop and maintain a network of medical and scientific consultants and provide training on protocol and therapeutic areas.
• Participate in investigator meetings, present safety and protocol updates, and support subject recruitment and retention.
• Assist in site selection, investigator networking, and the creation of medical monitoring plans.

Required profile

• Medical degree (MD, DO, or equivalent) with board certification in Oncology or related specialty.
• Extensive experience (typically ≥8 years) in clinical research, including medical monitoring of oncology trials.
• Proven ability to work independently in a remote, matrix‑managed environment.
• Strong communication skills for interaction with sponsors, investigators, and cross‑functional teams.

Required skills

• Good Clinical Practice (GCP) compliance.
• Clinical trial monitoring and adverse event evaluation.
• Protocol development and review.
• eCRF management.