Medical Monitor – Oncology

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

📋 Description

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

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

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

• Offer medical insights into eligibility evaluations, protocol deviations, participant safety concerns, and trial-specific medical issues.

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

• Create and present medical and therapeutic area training sessions for investigators and study teams.

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

• Engage in bid defense meetings and proposal initiatives.

• Support pharmacovigilance efforts.

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

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

• Ensure that trial conduct and medical oversight are in compliance with approved protocols, regulatory standards, 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 industries 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 with international, cross-functional teams.

• Proficient in Microsoft Office applications.

• Comfortable utilizing clinical trial systems and digital collaboration tools.

🏝️ Benefits

• International team of medical professionals.

• Opportunity to leverage oncology expertise across global studies.

• Collaboration with experienced colleagues.

• Chance to contribute to the development of new treatment options for patients.