Clinical Trial Coordinator - Paris, France (Hybrid) - FSP

I contribute to clinical research with expertise and empathy. And I do it
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Clinical Trial Coordinator - Paris, France (Hybrid) - FSP
Primary Location: France, Remote Job ID R0000046676 Category Project Leadership Date Posted 10/08/2026
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Success profile
About this role
Potential career path
Employee insights
Why Project Leaders work at Parexel
Learn about our culture
Overview
As a part of the global Project Leadership group at Parexel, you are responsible for leading cross-functional teams to deliver high-quality and patient-focused clinical trials and help bring life-changing treatments to market faster. You collaborate with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets. The role requires strong leadership and communication skills, the ability to work under pressure, and a passion for improving patients' lives.
In return, Parexel offers a supportive work environment, and a high degree of empowerment and accountability to lead your studies. Within this role, you work with a diverse set of clients and therapeutic areas, and you are encouraged to take on new challenges and pursue your interests.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
Adaptable
Communicator
Collaborative
Leadership
Proactive
Problem-solver
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About This Role
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 seeking a Clinical Trial Coordinator (Clinical Trial Assistant, Study Coordinator, Project Support Associate or similar) to join our team in a hybrid capacity, 2 – 3 days/week in Paris, France.
As a Clinical Trial Coordinator, you will play an important role in supporting the successful delivery of clinical research studies from study start-up through study closure. You will work closely with Clinical Research Managers and cross functional stakeholders to ensure effective study administration, regulatory compliance, document management, financial coordination, and operational support. Responsibilities include trial and site administration, maintenance of study tracking systems, support of budgeting and payment activities, document management, and stakeholder coordination, with opportunities to further develop your expertise within clinical research operations.
You'll join a fast paced, growth-oriented environment focused on advancing high-quality clinical research that brings innovative therapies to patients. Working within a dedicated sponsor partnership, you will collaborate with experienced industry professionals while gaining exposure to clinical trial processes that support meaningful scientific and medical progress. The Clinical Trial Coordinator role offers opportunities to expand your skills and explore long term career paths within clinical research.
Key Responsibilities
Support Clinical Research Managers and study team members throughout the clinical trial lifecycle from study start-up to study closure.
Provide trial and site administration and operational support.
Collaborate with finance and budgeting representatives to support study related financial activities.
Coordinate and support study meeting planning activities.
Interact with internal and external stakeholders, including study sites and vendors, in support of clinical study objectives.
Track and report negotiation activities related to study operations.
Ensure compliance with applicable financial procedures.
Maintain study tracking tools and systems.
Collate, distribute, and archive clinical trial documentation.
Assist with electronic Trial Master File reconciliation activities.
Support budgeting, agreement, and payment processes in collaboration with relevant stakeholders.
Candidate Profile
You'll Thrive In This Role If You Bring
Strong organizational, time management, interpersonal, and conflict management skills.
Experience working in clinical research, healthcare, or a regulated environment.
The ability to collaborate across teams and communicate effectively with both internal stakeholders and external customers, including sites and investigators.
A patient focused mindset and strong attention to detail.
Comfort working with clinical trial documentation, tracking systems, and study support processes.
Required Qualifications
B.A./B.S. degree, preferably in Life Sciences, or equivalent healthcare experience.
Minimum 1 to 2 years of experience in Clinical Research in a similar role.
Good understanding of global and country/regional clinical research guidelines.
Experience working with clinical trial documentation, tracking tools, and electronic Trial Master File processes.
Strong communication, organizational, and problem-solving skills.
Fluent in local language and business proficient in English, both written and verbal.
Ability to work independently.
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.
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Potential Career Path
Parexel offers a growth path with diverse therapeutic areas and clients, so you can grow according to your interests.
Associate Project Leader
Project Leader
Senior Project Leader
Associate Project Director
Project Director
Director, Project Leadership
Senior Director, Project Leadership
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Employee Insights
Donata about the team culture and career growth
Donata Juske | Senior Project Leader
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Helen on the diverse work experience
Helen Buttinger | Associate Project Director
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Briar on creating work-life balance
Briar Jallad | Associate Director, Project Management
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Why Project Leaders work at Parexel
Patient-led in everything we do
We lead and drive the success of clinical trials and feel the satisfaction of seeing the positive impact of our work on patients' lives.
Supportive and inclusive environment
We build a culture where relationship building is a priority for the success of our cross-functional teams and our client interaction.
Accountability and growth
We provide Project Leaders with the responsibility and empowerment to turn challenges into achievements and development opportunities.
Flexible work arrangements
We offer remote, in-office and hybrid roles to balance work and personal life depending on your needs.
Varied project experience
We continuously learn from a broad exposure of small biotech or large pharma clients, different therapeutic areas and innovative trial design.
Career progression
We offer various career paths, including enhancing your position, moving into management, or developing into other areas of the business.
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Learn About Our Culture
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Meet Iram Qayum, An Associate Project Director
With 18 years in clinical research, Iram Qayum, Associate Project Director at Parexel, leads clinical trials with a focus on operational excellence and patient care. Discover her journey of leadership, growth, and making an impact in the healthcare industry.
Learn More
A day in a life of a Project Leader
Christine and Ewa share what a Project Leader d

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