Medical Monitor – Oncology

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

📋 Description

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

• Offer medical oversight during clinical trials, adhering to protocols, regulations, and ICH-GCP standards.

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

• Provide medical insights during eligibility evaluations, protocol deviations, participant safety concerns, and 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.

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

• Prepare and conduct medical and therapeutic-area training sessions.

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

• Engage in bid defense meetings and proposal initiatives.

• Facilitate Pharmacovigilance activities.

• Identify risks associated with medical trials and collaborate on mitigation and escalation strategies.

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

• Ensure 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 within the pharmaceutical or CRO industry is advantageous.

• Fluent in written and spoken English.

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

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

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

• Proficient in Microsoft Office applications.

• Comfortable utilizing clinical trial systems and digital collaboration tools.

🏝️ Benefits

• Join an international team of medical professionals.

• Opportunity to leverage oncology expertise in global studies.

• Collaborate with experienced colleagues.

• Contribute to the introduction of new treatment options for patients.