Clinical Research Associate Jobs in Île-de-France, France

We are now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in France. This is a remote based position with travel to sites for monitoring visits.

TFS HealthScience's Clinical Development Services (CDS) Ophthalmology team is building a network of Freelance Senior Clinical Research Associates (0.4 FTE) based in France to support an anticipated ophthalmology project. The role involves initiation, on-site and/or remote monitoring, and closeout of study sites, including unmasked CRA support, investigational product accountability, and protocol compliance oversight.

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.

The (Senior) Clinical Research Associate (CRA) will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.

We are currently hiring a Freelance Clinical Research Associate in France for circa. 0.1 FTE to join our amazing team! In this role, you will have the opportunity to manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files.

As part of the clinical trials conducted by Epicentre/MSF on Ebola caused by the Bundibugyo virus (BDBV) in the Democratic Republic of the Congo (DRC), and potentially in other countries, the Clinical Research Associate (CRA) ensures the quality and regulatory compliance of studies in accordance with applicable International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines. The CRA conducts clinical monitoring activities, oversees the management of investigational products i

CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. CRA performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/onco-hematology clinical trials within the assigned country/region.

At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership , working closely with a strategic sponsor in a highly collaborative and quality-focused environment. This evergreen posting is part of our ongoing talent pipeline strategy and enables interested candidates to be considered for future opportunities aligne

Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study

Fortrea is recruiting! Fortrea in Paris is looking for a Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated.

This role will be responsible for site monitoring activities to ensure the overall integrity of study implementation and adherence to study protocol at assigned clinical sites. This role will be to work on medical device trials in Cardiology.

IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers.

Bring your monitoring expertise to the forefront of innovation. We are looking for a Contractor Clinical Research Associate (CRA) to join our A-team (hybrid).

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study

Clinical Research Associate I on Thermo Fisher Scientific's Clinical Operations team, supporting global pharmaceutical and biotech trials. Conducts remote and on‑site monitoring visits, ensures protocol and ICH‑GCP compliance, and manages documentation and risk‑based monitoring activities.

We have a Clinical Research Associates (or Senior CRAs depending on experience) open in France. Flexible locations can be considered, ideally close to a city with good connections for national travel.

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study

Clinical Research Team at Thermo Fisher Scientific supports global pharmaceutical studies. The Assistant Clinical Research Associate provides site preparedness, logistical support, and remote monitoring assistance across study start‑up, recruitment, and close‑out phases.