Global Oncology Medical Monitor

Psi CRO; England; On-site; GBP 85,000 - 120,000; Full time

Job summary

PSI CRO is seeking a Medical Monitor (Oncology) to oversee medical aspects of global clinical trials, ensuring participant safety and scientific quality. You will collaborate with sponsors, investigators, sites, and cross-functional teams to support oncology studies.

You should bring MD with oncology board certification and strong English communication. Prior CRO/pharma experience is a plus; stay aligned with protocol, safety data, and regulatory expectations.

Qualifications

• MD degree and oncology board certification.
• Experience as a practicing oncologist is preferred.
• Full professional proficiency in English (written and spoken).
• Experience in clinical research or CRO/pharma is a plus.

Responsibilities

• Serve as primary medical contact for trials coordinating with sponsors, investigators, and sites.
• Provide medical oversight in trials per protocol, regulations, and ICH-GCP.
• Address medical questions from investigators, sites, sponsors and vendors.
• Contribute to eligibility assessments, protocol deviations and safety issues.
• Contribute to trial documents: protocols, ICFs, reports, presentations.

Skills

Medical knowledge

Analytical thinking

Attention to detail

Communication skills

Team collaboration

Office software

Clinical trial systems

Education

Medical Doctor degree

Board certification in Oncology

Tools

Microsoft Office

Clinical trial systems

Job description

PSI CRO is seeking a Medical Monitor (Oncology) to oversee medical aspects of global clinical trials, ensuring participant safety and scientific quality. You will collaborate with sponsors, investigators, sites, and cross-functional teams to support oncology studies.

You should bring MD with oncology board certification and strong English communication. Prior CRO/pharma experience is a plus; stay aligned with protocol, safety data, and regulatory expectations.