Medical Monitor – Oncology

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

📋 Description

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

• Ensure medical oversight throughout 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 regarding eligibility evaluations, protocol deviations, participant safety issues, and other trial-specific concerns.

• Apply medical expertise 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 medically relevant trends, risks, or quality concerns.

• Create and deliver medical and therapeutic-area training to investigators and study teams.

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

• Engage in bid defense meetings and proposal activities.

• Support Pharmacovigilance initiatives.

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

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

• Help ensure trial execution and medical oversight adhere to approved protocols, regulatory standards, and quality benchmarks.

⛳️ 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 thinking, and meticulous attention to detail.

• Effective communication and presentation skills, with the capability to convey complex medical information to diverse stakeholders.

• Collaborative and solution-focused approach to working in international, cross-functional teams.

• Proficient in Microsoft Office applications.

• Comfort with clinical trial systems and digital collaboration tools.

🏝️ Benefits

• Work with an international team of medical professionals.

• Opportunity to leverage oncology expertise across global studies.

• Collaborate with experienced colleagues.

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

• Be part of an inclusive culture and environment where colleagues feel welcomed and valued.