Clinical Research

• 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 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
• 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.

Remote Clinical Research jobs in Portugal

Medical Monitor – Oncology

Scientific Director – SERM, Clinical Safety, Pharmacovigilance

Clinical Research Associate II

Freelance Clinical Research Associate

Clinical Research Associate II – Spanish, Portuguese, English

Clinical Research Associate II – Spanish, Portuguese, English