Medical Monitor – Oncology

This is a fully remote position, open to applicants in Czechia.

📋 Description

• Act as the main medical contact for sponsors, internal project teams, investigators, and trial sites.

• Provide medical oversight throughout clinical trials in alignment with protocols, regulations, and ICH-GCP standards.

• Address medical inquiries from investigators, sites, sponsors, project teams, and third-party vendors.

• Offer medical insights regarding eligibility assessments, protocol deviations, participant safety concerns, and other trial-specific issues.

• Contribute medical knowledge to clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations.

• Review and evaluate clinical and safety data to ensure participant safety and identify medically relevant trends, risks, or quality issues.

• Prepare and conduct medical and therapeutic-area training for investigators and study teams.

• Assist in the review of medical data and the assessment of aggregated clinical trial information.

• Take part in bid defense meetings and proposal-related activities.

• Support Pharmacovigilance efforts.

• Identify medical trial risks and work collaboratively on mitigation and escalation strategies.

• Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees.

• Ensure that trial conduct and medical oversight adhere to approved protocols, regulatory obligations, and quality benchmarks.

⛳️ Requirements

• Medical Doctor degree.

• Board certification in Oncology.

• Prior experience as a practicing Oncologist.

• Previous involvement in clinical research or within the pharmaceutical or CRO industry is advantageous.

• Full professional proficiency in both written and spoken English.

• Strong medical judgment, analytical skills, and meticulous attention to detail.

• Excellent communication and presentation abilities, capable of conveying complex medical information to various stakeholders.

• A collaborative and solution-focused mindset when working within international, cross-functional teams.

• Proficiency in Microsoft Office applications.

• Comfort with clinical trial systems and digital collaboration tools.

🏝️ Benefits

• An international team of medical professionals.

• The chance to apply oncology expertise across global studies.

• Collaboration with seasoned colleagues.

• Opportunity to contribute to the introduction of new treatment options for patients.