Clinical Trial Liaison

ICON San Antonio; Paris; Hybrid; EUR 90,000 - 120,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Country-specific benefits

Job summary

ICON is seeking a field-based Clinical Trial Liaison in France to support clinical trials across Europe. You will engage investigators and site teams, provide scientific guidance, and help drive patient enrolment while collaborating with sponsors and cross-functional teams.

The role requires travel up to 75% nationally and internationally, with a mix of home or office-based work. A doctoral degree and strong clinical research experience are essential, along with fluent English and French

Qualifications

• Doctoral degree such as MD, PharmD or PhD.
• Experience in clinical research within Pharma, Biotech or CRO environments.
• Strong scientific and medical knowledge with understanding of clinical development.
• Established scientific and clinical network in Europe with networking and negotiation skills.
• Excellent communication and presentation in English and French medical language; additional EU languages are an advantage.
• Ability to interpret complex medical data and apply scientific knowledge.
• Strong analytical, problem-solving and critical-thinking skills.
• Proactive, self-motivated and able to work independently and collaboratively.

Responsibilities

• Build relationships with investigators, site staff and stakeholders to support trial delivery.
• Provide scientific, clinical and protocol training to study teams.
• Develop site and study-level enrolment strategies to improve recruitment.
• Collaborate with cross-functional teams to translate best practice into local action.
• Represent the study at site visits, project meetings and conferences.
• Support continuous improvement of enrolment processes and trial outcomes.

Skills

Communication skills

English/French medical language

Networking & negotiation

Analytical thinking

Independent & collaborative working

Education

Doctoral degree

Job description

Clinical Trial Liaison - France

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

ICON is seeking a field-based Clinical Trial Liaison in France to support clinical trials across Europe by engaging investigators and site teams, providing scientific and clinical guidance, and helping drive successful patient enrolment.

In this role, you will work closely with study sites, sponsors and cross-functional teams to improve site engagement, strengthen recruitment strategies and ensure study teams have a clear understanding of trial design, protocol requirements and enrolment goals.

What you will be doing

• Build strong relationships with investigators, site staff and key stakeholders to support trial delivery and patient recruitment.
• Provide scientific, clinical and protocol training to study teams, ensuring clear understanding of study design and procedures.
• Develop and optimise site and study-level enrolment strategies to improve recruitment and retention.
• Collaborate with cross-functional teams to translate best practice into local, practical action.
• Represent the study at site visits, project meetings, industry events and conferences.
• Support continuous improvement of enrolment processes and trial outcomes.

What you will bring

• Doctoral degree such as MD, PharmD or PhD.
• Experience in clinical research within Pharma, Biotech or CRO environments, ideally in scientific, clinical operations or enrolment-focused roles.
• Strong scientific and medical knowledge, with an understanding of clinical development and local healthcare landscapes.
• Established scientific and clinical network in Europe, with strong networking, influencing and negotiation skills.
• Excellent communication and presentation skills in English and French medical language; additional EU languages are an advantage.
• Ability to interpret complex medical data and apply technical, scientific and clinical knowledge.
• Strong analytical, problem-solving and critical-thinking skills, with a detail-oriented approach to accuracy and compliance.
• Proactive, self-motivated and able to work both independently and collaboratively.

This home- or office-based role requires national and international travel of up to approximately 75%. Candidates should be based within easy access of an international airport.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Inclusion & Belonging

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here