Senior Clinical Research Associate; Oncology; Paris Region, France; Home-based; 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.

Parexel is a leading global clinical development partner delivering insight-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®.

We are seeking a Senior Clinical Research Associate (SCRA) to join our team in France in a remote/home-based capacity.

As a Senior Clinical Research Associate, you will play a critical role in advancing oncology research by ensuring clinical trial quality, data integrity, patient safety, and regulatory compliance at the site level. Working within a sponsor-dedicated model, you will oversee monitoring activities across assigned investigator sites, collaborating closely with site personnel, investigators, and project teams to support successful study delivery.

This position offers the opportunity to contribute directly to the development of innovative therapies while building strong partnerships with sites and stakeholders. You will leverage your expertise in oncology clinical trials, including RECIST criteria, to support study execution through a combination of remote and on-site monitoring activities. Your work will help ensure that studies remain inspection-ready, compliant, and focused on delivering high-quality outcomes for patients.

You will join a collaborative, growth-oriented environment where your contributions are highly visible and where continuous learning, professional development, and meaningful impact are part of everyday work.

• Ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and company procedures across assigned sites.

• Evaluate site performance and provide recommendations for site-specific actions, escalating significant issues and supporting development of corrective action plans when required.

• Verify that informed consent processes are appropriately conducted and documented for each study participant.

• Assess patient safety and clinical data integrity by identifying protocol deviations, violations, pharmacovigilance concerns, and other site-level risks.

• Conduct monitoring activities through remote and on-site methods in accordance with the Clinical Monitoring Plan and Study Monitoring Plan.

• Perform source document review and verification, ensuring clinical data entered into case report forms is accurate, complete, and supported by source documentation.

• Manage protocol deviation reporting, follow-up activities, and timely resolution of data queries.

• Review investigational product accountability, storage, security, dispensing, administration, reconciliation, and related documentation where applicable.

• Document monitoring…