Medical Advisor – Oncology (Clinical Trials)

Start: asapProject Duration: around 9-12 monthsFocus: Clinical Trials (Solid Tumors)

We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support and medical monitoring.

Key Responsibilities

Serve as medical advisor/medical monitor for assigned oncology clinical trialsProvide protocol guidance, inclusion/exclusion decisions, and patient safety support to study teams and investigative sitesPerform medical review of protocols, IBs, CRFs, CSRs, AEs and SAEsSupport safety reviews, signal evaluation, and collaboration with PharmacovigilanceParticipate in study meetings and Investigator MeetingsProvide timely support for urgent protocol‑related queries (per local regulations)

Requirements

MD with formal training and relevant experience in Oncology5–7+ years of experience supporting oncology clinical trialsStrong experience in solid tumorsConfident working in global, cross‑functional teams

IQVIA 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.com

IQVIA 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.