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Medical Monitor – Oncology
PSI CRO AG. Serve as primary medical point of contact for sponsors, internal project teams, investigators, and trial sites .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in medical oversight and clinical trial management, ensuring compliance with protocols and regulatory standards while effectively communicating complex medical information to diverse stakeholders. Proficient in analyzing clinical data and contributing to clinical development plans and safety assessments.
Highest-signal resume keywords
Medical OversightClinical Trial ManagementOncology Board CertificationClinical Research ExperienceMedical Data Analysis
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Medical Doctor DegreeOncology ExpertiseClinical ResearchMedical JudgementAnalytical ThinkingAttention to DetailProtocol ComplianceSafety MonitoringRisk AssessmentMedical Writing
Soft Skills
Clear CommunicationPresentation SkillsCollaborative ApproachSolution-Oriented Mindset
Tools & Technologies
Clinical Trial SystemsDigital Collaboration ToolsMicrosoft Office
Certifications & Qualifications
Board Certification in Oncology
Industry Keywords
ICH-GCP RequirementsPharmacovigilanceClinical Development PlansEligibility AssessmentsTrial-Specific Medical Matters
About the role
Key responsibilities & impact- Serve as primary medical point of contact for 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 vendors
- Provide medical input into eligibility assessments, protocol deviations, participant safety issues, and 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 relevant trends, risks, or quality concerns
- Prepare and deliver medical and therapeutic-area training
- 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
- 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