Clinical Research Associate Jobs in Nouvelle-Aquitaine, France

Clinical Operations at Worldwide Clinical Trials is building a global CRO that innovates in oncology and hematology. The Senior Clinical Research Associate drives site qualification, monitoring, and close‑out visits, mentors junior CRAs, and ensures protocol compliance and data integrity.

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.

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.

Clinical Payments team ensures accurate and timely financial transactions for clinical research sites and sponsors. The Associate monitors ticket queues, responds to payment inquiries, prepares remittance documentation, and supports system migration and study reconciliation tasks.

Clinical Assessment Technologies (CAT) team drives operational excellence for clinical assessment technology studies across global trials. The Associate Director leads end-to-end CAT study operations, overseeing resource planning, vendor coordination, compliance, and financial tracking while driving process improvements.

Research Associate III (Epidemiologist) – Real World Science at Thermo Fisher Scientific. This remote role across Europe supports de novo data collection projects, drafting protocols, CRFs, surveys, and reports.

TMF Operations team ensures trial documentation accuracy, compliance, and quality across global clinical research studies. The Senior Associate II manages TMF operations, conducts quality control, prepares KPI reports, and supports regulatory inspections while collaborating with project teams and sponsors.

Clinical Content & Terminology Senior Associate at athenahealth, Inc. works within the Chief Medical Officer Organization to research, develop, and maintain clinical content and terminology libraries that support global documentation needs. The role creates specialty‑specific content assets, validates standardized code mappings (SNOMED, LOINC, CPT, ICD‑10), and partners with product, technical writing, and external vendors to deliver updates for new workflows.

IQVIA’s Clinical Research team in Bordeaux drives the execution of clinical trials that bring innovative therapies to patients. The Coordinator supports investigators by managing study documentation, coordinating logistics, and ensuring participant safety and data integrity.

Clinical Research Nurse role in Bordeaux, France. Part-time 10 days, 8 hours/day, reviewing patient notes and extracting data for clinical studies.

Opportunity in Clinical Research at IQVIA. Part-time role supporting a clinical trial in Bordeaux, 10 days, 8 hours/day.

Field monitor for clinical trials, ensuring data quality, GCP compliance, and regulatory documentation. Provide oversight, training, and process improvements.

As the Clinical Research Director, you will spearhead cutting‑edge ophthalmic studies, guiding product development through trials, ensuring safety, efficacy, and regulatory compliance to advance eye care.

Clinical Data Management Team leads global clinical research programs, ensuring high‑quality trial data. The Principal Clinical Data Manager oversees multiple studies from start‑up to database lock, drives data integrity, regulatory compliance, and mentors the data management team.

Pierre Fabre seeks a Clinical Study Coordinator to support trial management, coordinate teams, draft regulatory documents, oversee CRO activities, manage budgets, and ensure GCP compliance. The role involves TMF management, insurance monitoring, and logistical support, with up to 2 remote days per week.

Thermo Fisher Scientific seeks a National Clinical Applications Specialist (LC-MS) to support Clinical Strategic Accounts across the U.S. The role focuses on advanced mass spectrometry technology, developing LC‑MS/MS methods for clinical research and toxicology, building experiments for new product introduction, and collaborating with key opinion leaders to generate marketing collateral. The specialist trains sales and customers on workflows, delivers product propositioning, and interacts with global commercial teams for pre‑ and post‑sales support.

Global Clinical Research Team drives life‑changing therapies through rigorous statistical science. The Senior Principal Statistician leads statistical activities across the full clinical study lifecycle, develops SAPs, oversees programming outputs, and mentors junior staff while collaborating with clinical, regulatory and programming partners.

Business Development team drives growth across the clinical research sector by forging new client relationships and expanding partnerships. The Senior Director leads complex sales initiatives, oversees proposal strategies, and represents the organization at industry events, collaborating with senior leadership on strategic opportunities.

Site Contracts Specialist at a global clinical research partner. Supports worldwide clinical trial operations by drafting, negotiating, and executing site contracts, ensuring regulatory compliance and financial alignment.

Business Development at Worldwide Clinical Trials, a global CRO focused on innovative clinical research. Leads sales calls, RFP coordination, and client strategy to drive revenue for phase I‑IV studies, while representing the company at trade shows and senior management meetings.