Medical Monitor – Oncology

PSI CRO AG

. Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites for medical matters related to clinical trials .

Posted 11/5/2026full-timeRemote • BelgiumMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical oversight for clinical trials, ensuring compliance with protocols, regulations, and ICH-GCP requirements. Proficient in analyzing clinical data and providing medical input to support participant safety and trial integrity.

Highest-signal resume keywords

Medical Doctor DegreeBoard Certification In OncologyClinical Research ExperienceMedical OversightProficiency In Microsoft Office

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical OversightClinical Data AnalysisEligibility AssessmentsProtocol DeviationsPharmacovigilanceMedical JudgementAnalytical ThinkingAttention To DetailClinical Trial SystemsDigital Collaboration Tools

Soft Skills

Clear CommunicationPresentation SkillsCollaborative ApproachSolution-Oriented Mindset

Certifications & Qualifications

Board Certification In Oncology

Industry Keywords

Clinical TrialsICH-GCPPharmaceutical IndustryCRO IndustryInvestigational BrochuresInformed Consent DocumentsSafety Monitoring BoardsAdvisory Boards

About the role

Key responsibilities & impact

Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites for medical matters related to clinical trials
Provide medical oversight throughout clinical trials in accordance with 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 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 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

What you’ll need

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
A 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

Comp & perks

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