Medical Monitor – Oncology

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

📋 Description

• Act as the main medical liaison for clinical trial sponsors, internal project teams, investigators, and trial sites regarding medical issues related to clinical trials.

• Ensure medical oversight during clinical trials in line with protocols, regulations, and ICH-GCP standards.

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

• Provide medical input on eligibility assessments, protocol deviations, participant safety concerns, and other trial-specific medical issues.

• Offer medical expertise for 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 relevant medical trends, risks, or quality issues.

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

• Assist with medical data review and evaluation of aggregated clinical trial data.

• Engage in bid defense meetings and proposal initiatives.

• Support Pharmacovigilance efforts.

• Recognize medical trial risks and work on mitigation and escalation strategies.

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

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

⛳️ Requirements

• Medical Doctor degree.

• Board certification in Oncology.

• Prior experience as a practicing Oncologist.

• Experience in clinical research or 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.

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

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

• Proficiency in Microsoft Office applications.

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

🏝️ Benefits

• International team of medical professionals.

• Opportunity to leverage oncology expertise in global studies.

• Collaboration with experienced colleagues.

• Chance to contribute towards providing new treatment options for patients.