Medical Monitor, Oncology

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

📋 Description

• Act as the primary 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 plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations.

• Review and analyze clinical and safety data to ensure participant safety and identify medically pertinent trends, risks, or quality issues.

• Prepare and conduct medical and therapeutic-area training for investigators and study teams.

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

• Take part in bid defense meetings and proposal initiatives.

• Support Pharmacovigilance efforts.

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

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

• Ensure that trial execution and medical oversight adhere to approved protocols, regulatory requirements, and quality standards.

⛳️ Requirements

• Medical Doctor degree.

• Board certification in Oncology.

• Previous experience as a practicing Oncologist.

• Experience in clinical research or within the pharmaceutical or CRO sectors is an advantage.

• 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-oriented mindset when working within international, cross-functional teams.

• Proficient in Microsoft Office applications.

• Comfort with clinical trial systems and digital collaboration tools.

🏝️ Benefits

• Work within an international team environment.

• Opportunity to utilize oncology expertise across global studies.

• Collaboration with experienced colleagues.

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