Clinical Trial Liaison – France

• Develop and maintain peer-to-peer relationships with key opinion leaders, principal investigators, sub-investigators, and healthcare providers within oncology clinical research
• Lead site and patient engagement initiatives to improve operational excellence, trial performance, patient experience, and diversity and inclusion within clinical studies
• Partner with cross-functional stakeholders to establish and achieve clinical operations objectives, work plans, recruitment timelines, and study deliverables
• Develop and execute territory plans aligned with broader site engagement strategies
• Identify, communicate, and share clinical research insights and emerging issues from research sites and healthcare providers with study teams
• Support clinical study education activities for healthcare professionals and community stakeholders around clinical trial sites
• Deliver scientific presentations and provide clinical information in response to unsolicited requests within academic, community, and healthcare settings, as appropriate
• Maintain current expertise in oncology, relevant research trends, disease management practices, and the competitive landscape
• Collaborate with internal and external stakeholders to strengthen site engagement strategies and enhance patient outcomes in clinical trials
• Support study-related materials, advisory activities, medical congress engagements, and training initiatives while ensuring compliance with applicable regulations and company standards

• Advanced degree (PharmD, MD, PhD, or equivalent) with a minimum of 3 years of experience in oncology medicine, OR license as an RN, NP, CNP, PA, or equivalent with a Master's degree (or equivalent) and a minimum of 5 years of experience in oncology medicine
• Minimum of 2 years of experience as a Medical Science Liaison or in a comparable industry or clinical role
• Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
• Demonstrated ability to analyse and communicate complex scientific and medical information to a variety of audiences
• Strong communication, presentation, organizational, negotiation, and problem-solving skills
• Excellent command of spoken English
• Valid driver's license and ability to travel approximately 60% of the time
• Experience working in clinical research, oncology, healthcare, or another regulated environment
• Ability to collaborate across functions and build trusted relationships with healthcare professionals and research sites
• Comfort working with digital platforms, scientific data, and clinical research processes
• Experience in solid tumors, targeted therapies, or related oncology specialties
• Strong understanding of healthcare systems, clinical practice trends, and oncology research environments
• Established credibility and success in developing relationships with external experts and opinion leaders
• Familiarity with field-based medical, scientific, or clinical engagement activities
• Experience supporting clinical research programs within oncology therapeutic areas

• Medical Plan
• Life Assurance
• Pension
• Comprehensive benefits package for eligible employees
• Flexibility
• Growth opportunities