IQVIA
Medical Advisor – Oncology (Clinical Trials)
- Start: asap
- Project Duration: around 9-12 months
- Focus: 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 trials
- Provide protocol guidance, inclusion/exclusion decisions, and patient safety support to study teams and investigative sites
- Perform medical review of protocols, IBs, CRFs, CSRs, AEs and SAEs
- Support safety reviews, signal evaluation, and collaboration with Pharmacovigilance
- Participate in study meetings and Investigator Meetings
- Provide timely support for urgent protocol‑related queries (per local regulations)
Requirements
- MD with formal training and relevant experience in Oncology
- 5–7+ years of experience supporting oncology clinical trials
- Strong experience in solid tumors
- Confident 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.
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