Clinical Research Associate Jobs in Rhône-Alpes, France

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology and onco‑hematology trials, ensuring GCP compliance and site performance. The role monitors sites, manages data quality, and collaborates with regional study teams to meet milestones.

BeOne Medicines I GmbH’s Clinical Research Associate team drives oncology trial excellence by monitoring sites, ensuring GCP compliance, and managing data quality. The role conducts site selection, initiation, routine and closeout visits, documents findings, and collaborates with regional study managers to meet milestones.

Clinical Monitoring and Site Management team at Premier Research supports biotech, medtech, and specialty pharma partners to launch and oversee clinical sites. The role prepares and submits regulatory applications, negotiates contracts and budgets, and conducts site identification and monitoring to ensure data integrity and patient safety.

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.

Join IQVIA as a Trainee Clinical Research Associate in the Italian-speaking region of Switzerland. This role offers career growth in clinical research, with responsibilities including site selection, monitoring, and collaboration with study sites.

The IQVIA™ Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future. You will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials.

Senior Clinical Research Associate (Level I) at Thermo Fisher Scientific’s PPD Argentina team, responsible for monitoring investigator sites using a risk‑based approach, ensuring protocol and ICH‑GCP compliance, and maintaining audit readiness. The role involves remote and occasional on‑site visits, data accuracy checks, and collaboration with clinical teams to resolve findings.

Senior Clinical Research Associate (Level I) at Thermo Fisher Scientific’s PPD Argentina team, responsible for monitoring investigator sites with a risk‑based approach, ensuring protocol and ICH‑GCP compliance, and maintaining audit readiness. The role involves remote and occasional on‑site visits, data accuracy checks, and collaboration with clinical teams to resolve findings.

Thermo Fisher Scientific’s PPD Argentina team seeks a Senior Clinical Research Associate to drive risk‑based monitoring across global trials. The role involves remote and occasional on‑site visits to ensure protocol compliance, data integrity, and audit readiness while collaborating with investigators and sponsors.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.

Associate Clinical Development Director (Neurosciences) at Novartis leads scientific and clinical strategy for assigned trials, overseeing trial documents, regulatory submissions, and safety reporting. The role requires advanced life sciences degree and 5+ years in clinical research across Phases I-IV, with at least 2 years of end-to-end trial execution in a global pharmaceutical setting.

Thermo Fisher Scientific team advancing clinical research supports project documentation, supply chain coordination, and service delivery for clinical trials. The Project Support Associate manages planning, cross‑functional coordination, and quality standards while generating reports and liaising with clients.

Thermo Fisher Scientific’s Clinical Services team empowers global clinical research. As a Project Support Associate, you manage documentation, coordinate supply chain activities, and ensure timely delivery of services for clinical trials.

Global Client Services at Thermo Fisher Scientific supports clinical research by managing project documentation and supply chain activities. The Project Support Associate partners with internal project managers, maintains study filing systems, creates operational documentation, and uses planning tools to track progress and ensure timely delivery.

Global Client Services at Thermo Fisher Scientific supports clinical research by managing project documentation and coordinating supply chain activities. The Project Support Associate partners with internal project managers to maintain study filing systems, create operational documentation, and ensure GMP compliance while tracking project timelines.

CSL’s R&D team seeks an Associate Director of Patient Engagement to lead relationships with advocacy groups, guide trial design, and integrate patient insights into clinical research. The role blends strategic advisory, partnership development, and data analysis across global sites, ensuring patient-centric approaches in trial planning and recruitment.

Clinical Development Medical Director (CDMD) for Immunology leads program-level clinical activities, including protocol sections, data review, regulatory dossiers, and publications. The role drives execution with global line functions, Global Trial Directors, and regional medical associates, overseeing medical and scientific review of trial data and serving as study medical monitor.

Clinical Development Medical Director - Cardiovascular at Novartis leads clinical programs in cardiovascular therapeutics, overseeing protocol development, data review, regulatory documentation, and publications. The role drives execution with global line functions, trial directors, and regional associates, and conducts medical and scientific reviews of trial data.

Clinical Development Medical Director – CRM leads a clinical program section or large trial, providing strategic medical input and overseeing deliverables such as protocols, data reviews, regulatory dossiers, and publications. The role partners with global line functions, Global Trial Directors, and regional medical associates to execute program sections, conduct medical and scientific reviews with Clinical Scientific Experts, and monitor safety through the Safety Management Team.

Clinical Development Medical Director at Novartis leads end‑to‑end clinical development for cardiovascular programs. The role oversees clinical leadership, strategic medical input, and regulatory documentation across global teams.