As a Clinical Research Associate II, you will monitor clinical studies at investigative sites, ensuring they're conducted and reported per protocol. You'll coordinate activities, identify investigators, and help prepare regulatory submissions with an impeccable eye for detail. You will identify risks and take responsibility for the quality of your work.
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Join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a CRA homebased in France. You will have ownership of investigator sites for assigned studies and be responsible for the successful management of the site right through to close-out. You will also plan and conduct various site visits, develop effective relationships with investigator site staff, and ensure integrity of clinical data.
As a (CRA I/II) you will be supporting a long-term partnership with one of the most established pharmaceutical companies in the industry. Within this program you will find a culture focused on teamwork and camaraderie; where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology, women’s health, and cell & gene therapy.
Parexel is seeking Clinical Research Associates with at least 12 months recent oncology experience to be dedicated to a single sponsor. Manageable sites and protocols are the mantra, offering exciting challenges with time for your outside life. The role involves site management and monitoring activities across assigned oncology studies, working with industry leaders and world-class technology.
You will play a vital client facing line management role, embedded in our clients business and will be responsible for the management of day to day clinical trial quality activities, training, and promoting efficiency in project work while partnering with a well-known global pharmaceutical company.
As a Clinical Research Associate, you will perform site qualification, initiation, and closeout visits, ensuring regulatory and protocol compliance. Generate queries and manage resolutions with site personnel, documenting activities. Ensure proper recruitment/maintenance plans and act as the primary liaison with site personnel. Manage site's study regulatory documents and assist with audit preparation.
Monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all activities to set up and monitor a study. You will identify investigators and help prepare regulatory submissions.