Medical Monitor (Oncology)

PSI CRO

About The Position

PSI is seeking a Medical Monitor to join its international Medical Monitoring team. The role provides medical oversight and expertise across global oncology clinical trials, working with study sponsors, investigators, sites, project teams, and other clinical research professionals. The position supports participant safety, scientific and medical quality, and successful study delivery, applying clinical oncology experience to international research and the development of new treatments.

Requirements

Medical Doctor degree.
Board certification in Oncology.
Previous experience as a practicing Oncologist.
Full professional proficiency in written and spoken English.
Strong medical judgment, analytical thinking, and attention to detail.
Clear communication and presentation skills, including the ability to explain complex medical information to different stakeholders.
Collaborative and solution-oriented approach to working within international, cross-functional teams.
Proficiency in Microsoft Office applications and confidence working with clinical trial systems and digital collaboration tools.

Nice To Haves

Previous experience in clinical research or the pharmaceutical or CRO industry.

Responsibilities

Serve as the primary medical contact for sponsors, internal project teams, investigators, and trial sites on medical matters related to trial conduct, protocols, and GCP guidelines.
Provide medical oversight throughout clinical trials in accordance with protocols, applicable regulations, and ICH-GCP requirements.
Respond to medical questions from investigators, sites, sponsors, project teams, and third-party vendors.
Provide medical input on 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.
Prepare and deliver medical and therapeutic-area training to investigators and study teams.
Support medical data review activities and contribute to assessment of aggregated clinical trial data.
Participate in bid defense meetings and proposal activities.
Provide support for pharmacovigilance activities.
Identify medical trial risks and collaborate with relevant functions to define mitigation and escalation measures.
Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees, as applicable.
Help ensure trial conduct and medical oversight comply with approved protocols, regulatory requirements, and quality standards.