Clinical Research

• 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

Explore Medical Monitor – Oncology at PSI CRO AG. Review requirements and application details.

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