Medical Monitor, Oncology

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

📋 Description

• Act as the main medical liaison for clinical trial sponsors, internal project teams, investigators, and trial sites regarding medical issues pertaining to clinical trial execution in line with protocols and GCP guidelines.

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

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

• Offer medical insights on eligibility evaluations, protocol deviations, participant safety concerns, and other 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 support participant safety and detect medically relevant trends, risks, or quality issues.

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

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

• Engage in bid defense meetings and proposal initiatives.

• Contribute to Pharmacovigilance efforts.

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

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

• Help ensure that trial execution and medical oversight adhere to approved protocols, regulatory requirements, 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 sector is advantageous.

• Full professional proficiency in both 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 diverse stakeholders.

• A collaborative and solution-oriented mindset for working within international, cross-functional teams.

• Proficiency in Microsoft Office applications.

• Comfort in 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.