Clinical Trial Liaison - France (Remote) - FSP

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.

About the Role

We are registering interest for a Global Patient and Site Engagement Clinical Trial Liaison (CTL, Clinical Trial Liaison) to join our team in France, in a remote capacity. As a Global Patient and Site Engagement Clinical Trial Liaison, you will play a critical role in advancing oncology clinical research by driving site engagement, strengthening investigator relationships, and enhancing the patient experience across clinical trials.

This position serves as a strategic link between clinical research sites, healthcare professionals, and study teams, supporting trial execution through site and patient engagement initiatives, scientific exchange, operational collaboration, and regulatory compliance. You will work closely with key opinion leaders, principal investigators, sub-investigators, and cross-functional stakeholders to improve clinical trial performance, support patient recruitment objectives, and contribute to meaningful research outcomes for patients living with cancer.

You will join a fast-paced, growth-oriented environment where your expertise can influence trial success, improve access to innovative therapies, and support patient-centric clinical development. With opportunities to collaborate across global teams and deepen your oncology knowledge, this role offers an exciting pathway for professional growth within clinical research.

Key Responsibilities

• 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.

Candidate Profile

You’ll thrive in this role if you bring:

• Strengths in scientific communication, relationship building, strategic thinking, and stakeholder engagement
• Experience working in clinical research, oncology, healthcare, or another regulated environment
• The ability to collaborate across functions and build trusted relationships with healthcare professionals and research sites
• A patient-focused mindset combined with strong planning, organization, and attention to detail
• Comfort working with digital platforms, scientific data, and clinical research processes

Required Qualifications

• 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

Preferred Qualifications

• 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

Benefits and Compensation

• Medical Plan
• Life Assurance
• Pension

We offer a comprehensive benefits package to eligible employees, which includes life assurance and medical plan, and additional benefit offerings in accordance with the terms of our applicable plans.

If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.