Medical Monitor – Oncology
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Job Description
Medical Monitor overseeing oncology clinical trials for PSI, a global contract research organization. Providing medical oversight, safety review, and protocol expertise across international studies.
Responsibilities:
- Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators, and trial sites
- Provide medical oversight throughout clinical trials according to protocols, 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 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 and assessment of aggregated clinical trial data
- Participate in bid defense meetings and proposal activities
- Support Pharmacovigilance activities
- Identify medical trial risks and collaborate on mitigation and escalation measures
- Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees
- Help ensure trial conduct and medical oversight comply with approved protocols, regulatory requirements, and quality standards
Requirements:
- Medical Doctor degree
- Board certification in Oncology
- Previous experience as a practicing Oncologist
- Previous experience in clinical research or the pharmaceutical or CRO industry is a plus
- Full professional proficiency in written and spoken English
- Strong medical judgement, analytical thinking, and attention to detail
- Clear communication and presentation skills, with 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
- Confidence working with clinical trial systems and digital collaboration tools
Benefits:
- International team of medical professionals
- Opportunity to apply oncology expertise across global studies
- Collaboration with experienced colleagues
- Opportunity to contribute to bringing new treatment options to patients
- Inclusive culture and environment where colleagues feel welcomed and valued
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