Medical Monitor – Oncology

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

📋 Description

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

• Provide medical oversight throughout the duration of clinical trials in accordance with 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 other trial-specific medical issues.

• Contribute medical knowledge to clinical development strategies, 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 medical trends, risks, or quality issues.

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

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

• Participate in bid defense meetings and proposal-related activities.

• Support Pharmacovigilance initiatives.

• Recognize medical trial risks and collaborate on strategies for mitigation and escalation.

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

• Ensure trial execution and medical oversight adhere to 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.

• 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 diverse stakeholders.

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

• Proficient in Microsoft Office applications.

• Comfortable using clinical trial systems and digital collaboration tools.

🏝️ Benefits

• Join an international team of medical professionals.

• Opportunity to leverage oncology expertise on global studies.

• Collaborate with experienced colleagues.

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