Medical Monitor (Oncology)

PSI is seeking a Medical Monitor (Oncology) to join our international Medical Monitoring team.

In this role, you will provide medical oversight and expertise across global clinical trials, working closely with study sponsors, investigators, sites, project teams, and other clinical research professionals. Your contribution will help protect participant safety, maintain scientific and medical quality, and support the successful delivery of oncology studies.

This is an opportunity to apply your clinical oncology experience to international research and contribute directly to the development of new treatments for patients who need them.

Full-time employment

Responsibilities:

• Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines
• Provide medical oversight throughout the conduct of clinical trials, in accordance with the protocol, applicable regulations, and ICH-GCP requirements
• Respond to medical questions from investigators, sites, sponsors, project teams, and third-party vendors
• Provide medical input into eligibility assessments, protocol deviations, participant safety issues, and other trial-specific medical matters
• Contribute medical expertise to clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations
• Review and assess clinical and safety data to support participant safety and identify medically relevant trends, risks, or quality concerns
• Prepares and delivers medical training and/therapeutic area training to investigators and study teams
• Support medical data review activities and contribute to the assessment of aggregated clinical trial data
• Participate in bid defense meetings and proposal activities
• Provide support with Pharmacovigilance activities
• Identify medical trial risks, and collaborate with relevant functions to define appropriate mitigation and escalation measures
• Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees, as applicable.
• Help ensure that trial conduct and medical oversight activities comply with the approved protocol, applicable regulatory requirements, and quality standards