Medical Monitor – Oncology

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

📋 Description

• Act as the primary medical liaison for clinical trial sponsors, internal project teams, investigators, and trial sites concerning medical issues related to the conduct of clinical trials following established protocols and GCP guidelines.

• Ensure medical oversight throughout clinical trials, adhering to protocols, relevant regulations, and ICH-GCP standards.

• Address medical inquiries from investigators, sites, sponsors, project teams, and external vendors.

• Offer medical insights regarding eligibility evaluations, protocol deviations, participant safety concerns, and other trial-specific medical 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 enhance participant safety and discern medically significant trends, risks, or quality issues.

• Develop and deliver medical and therapeutic-area training for investigators and study teams.

• Assist with medical data review processes and the assessment of aggregated clinical trial data.

• Engage in bid defense meetings and proposal initiatives.

• Support Pharmacovigilance activities.

• Identify medical trial risks and collaborate with relevant departments on mitigation and escalation strategies.

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

• Help ensure that trial execution and medical oversight align with approved protocols, regulatory standards, and quality benchmarks.

⛳️ Requirements

• Medical Doctor degree.

• Board certification in Oncology.

• Prior experience as a practicing Oncologist.

• Experience 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 attention to detail.

• Effective communication and presentation skills, capable of simplifying complex medical information for various stakeholders.

• A collaborative and solution-focused attitude towards working within international, cross-functional teams.

• Proficiency in Microsoft Office applications.

• Comfort in utilizing clinical trial systems and digital collaboration tools.

🏝️ Benefits

• Competitive salary and performance-based incentives.

• Comprehensive health, dental, and vision insurance.

• Opportunities for professional development and continuing education.

• Flexible work arrangements and a supportive work environment.

• Access to cutting-edge research and clinical trial resources.