Medical Monitor

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

THE MEDICAL MONITOR ROLE

The Medical Monitor is a key clinical expert responsible for ensuring the medical and scientific integrity of clinical trials, overseeing patient safety, and supporting study teams in protocol execution. Reporting to the Vice President of Clinical Operations (EU), the Medical Monitor works closely with sponsors, investigators, and internal clinical teams to ensure the highest ethical, medical, and regulatory standards throughout the clinical trial lifecycle.

The role requires expertise in clinical trial design, medical data interpretation, and regulatory compliance, with a strong focus on patient safety, risk mitigation, and adherence to study protocols. 

KEY RESPONSIBILITIES

Medical Oversight & Patient Safety:

• Provide medical monitoring for clinical trials, ensuring the safety and well-being of study participants.
• Review and assess adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs), ensuring timely reporting and regulatory compliance.
• Serve as the primary medical contact for clinical sites and investigators, addressing protocol-related questions and safety concerns.

Clinical Trial Conduct & Compliance:

• Oversee study adherence to Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and local regulatory requirements.
• Participate in study start-up activities, including protocol development, investigator meetings, and regulatory submissions.
• Support the preparation and review of Clinical Study Reports (CSRs) and other regulatory documents.

Medical & Scientific Expertise:

• Provide medical input during study design, protocol development, and risk assessment to ensure scientific rigor and feasibility.
• Contribute to the development of investigator brochures, informed consent forms, and study-specific training materials.
• Assist in the review and interpretation of clinical trial data, ensuring accuracy and relevance.

Stakeholder Engagement & Communication:

• Collaborate with investigators, sponsors, clinical operations teams, and regulatory authorities to support study execution.
• Participate in safety review meetings, data monitoring committees (DMCs), and investigator meetings.
• Provide medical training to clinical research teams, ensuring alignment on trial protocols and safety procedures

Risk Management & Continuous Improvement:

• Identify and mitigate potential medical risks associated with clinical trial conduct.
• Support audit and inspection readiness, ensuring trial compliance with regulatory expectations.
• Contribute to process improvement initiatives, optimizing medical monitoring workflows and best practices.

DESIRED QUALIFICATION & EXPERIENCE 

• Medical degree (MD) is required; specialization in a relevant therapeutic area (e.g., oncology, cardiology, neurology) is a plus.
• Clinical experience and/or previous industry experience in medical monitoring or clinical research.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Experience in safety monitoring, pharmacovigilance, or clinical risk management.
• Ability to interpret clinical trial data, assess safety trends, and make informed medical decisions.
• Prior experience in sponsor, CRO, or regulatory interactions is preferred.

TECHINICAL COMPETENCES & SOFT SKILLS 

Technical competencies:

• Clinical trial medical monitoring and patient safety oversight.
• Adverse event and serious adverse event evaluation and reporting.
• Knowledge of clinical research methodologies, study design, and statistical concepts.
• Experience with regulatory requirements, pharmacovigilance, and safety reporting.
• Ability to review and interpret clinical data, protocols, and study reports.
• Proficiency in scientific writing and regulatory documentation.
• Fluent in English; additional European languages (e.g., French, German, Italian) are a plus.

Soft Skills:

• Strong communication and collaboration skills with cross-functional teams.
• Analytical and critical thinking to assess and interpret clinical data effectively.
• Detail-oriented and organized, ensuring accuracy in safety reporting and documentation.
• Problem-solving mindset, able to address challenges in clinical trial execution.
• Leadership and mentoring abilities, guiding clinical teams and investigators.
• Adaptability and flexibility to work in a dynamic, fast-paced environment. 

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