Clinical Research Associate Jobs in Centre, France

Global Clinical Operations (GCO) at Allucent drives clinical trial execution for biopharma partners. The CRA II/Sr. CRA independently monitors investigational sites across France, ensures protocol and GCP compliance, builds strong site relationships, and mentors junior CRAs.

IQVIA Biotech partners with visionary biotech companies to accelerate clinical development from early phase through global registrational studies. The Clinical Research Associate conducts site monitoring visits, manages recruitment plans, ensures regulatory compliance, and maintains trial documentation to support study execution.

IQVIA Biotech partners with visionary biotech companies to accelerate clinical development from early phase to global registrational studies. The Clinical Research Associate monitors sites, drives recruitment, manages protocol training, and ensures GCP/ICH compliance while maintaining TMF and ISF records.

Fortrea seeks a Clinical Research Associate I to manage site operations, monitor trials, ensure protocol compliance, review CRFs, handle SAE reporting, and train new staff. Requires 6 months related experience, English fluency, matrix environment proficiency, and a valid driver's license.

Clinical Research Associate I to monitor study sites, ensure data integrity, conduct visits, manage SAE reporting, support QA, travel required, 6 months experience, English fluency, regulatory knowledge, driver license.

Clinical Research Associate II – a role that bridges science and solutions, overseeing global clinical trials from site management to data integrity. The position requires a solid grasp of ICH‑GCP, clinical monitoring, and regulatory compliance, with a focus on detail, documentation, and effective communication.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Engage in structured training to gain knowledge and skills for independent clinical monitoring visits per protocol, SOPs, GCP, and regulatory requirements. Perform site monitoring, training, quality evaluation, data tracking, documentation, and project support under supervision.

IQVIA offers a 6‑month internship for aspiring Clinical Research Associates in Paris. Interns receive structured training in clinical monitoring, protocol compliance, and regulatory requirements, and support site visits, data management, and documentation under supervision.

Clinical Research team at AstraZeneca conducts global clinical trials to bring innovative medicines to patients. The Clinical Research Associate monitors study sites, ensures compliance with ICH/GCP guidelines, and collaborates with local study delivery teams to meet quality and timeline commitments.

AstraZeneca’s Clinical Research Associate team drives the delivery of cardiovascular, metabolic, respiratory, and immunology studies. The role monitors and manages site operations, ensuring GCP compliance and quality metrics while collaborating with monitors and local teams.

Inhouse Clinical Research Associate (IHCRA) at Novotech supports the clinical team in France, ensuring compliance with ICH GCP, local regulations, and company SOPs. The role coordinates Trial Master Files, manages the Clinical Trial Management System, and assists with site visits, IRB submissions, and document archiving.

Stryker Clinical Research team drives global clinical studies, ensuring quality and compliance across diverse therapeutic areas. As Lead CRA, you pilot site monitoring, mentor junior CRAs, and coordinate multi‑site operations, impacting study success worldwide.

IQVIA Clinical Functional Services Partnerships (FSP) builds dedicated clinical teams for single sponsors, delivering quality monitoring and training across France. The Junior CRA supports 1‑2 oncology, neurology, immunology or diabetes protocols, managing ~10 sites, driving recruitment plans, and creating monitoring reports.

IQVIA Clinical Functional Services Partnerships (FSP) team focuses on delivering high‑quality clinical research for a single sponsor, acting as the sponsor’s dedicated partner. The Experienced Clinical Research Associate manages site monitoring across France, drives recruitment plans, trains sites, and mentors junior staff while maintaining risk‑based monitoring practices.

IQVIA’s Clinical Research team in Illkirch‑Graffenstaden and Paris drives global drug development by ensuring sites execute trials per GCP and ICH standards. The role monitors site visits, manages recruitment plans, and maintains Trial Master Files to guarantee data integrity.

Senior Clinical Research Associate at Parexel, focused on oncology trials in the Paris region. The role ensures data integrity, GCP compliance, and remote monitoring of sites, collaborating closely with Site Managers and investigators.

IQVIA Clinical Functional Services Partnerships (FSP) team builds quality delivery for a single sponsor, focusing on oncology, neurology, immunology and diabetes studies. The CRA manages 15 sites across France, drives recruitment, conducts monitoring visits 6‑9 days/month, and mentors junior staff.

IQVIA’s Clinical Research team in France ensures study sites comply with GCP and ICH guidelines. The role conducts site monitoring visits, drives recruitment plans, administers protocol training, and maintains Trial Master File documentation.

Parexel’s Oncology Clinical Research team drives data integrity and compliance for oncology trials. The Senior CRA monitors sites virtually, ensures GCP adherence, resolves queries, and collaborates with site managers to keep studies on schedule.