Get new jobs by email
- ...to perform and coordinate all aspects of the clinical monitoring and site management process. The IVD Clinical Research Associate (CRA) is responsible for monitoring clinical trial testing sites to ensure compliance with Clinical Performance Study Protocol (CPSP), protocol...Remote job
- ...share potential solutions for improvements. Performs additional tasks as assigned by Clinical Lead or Clinical Manager of CRAs (CM-CRA) (e.g. trip report review, newsletter creation, lead CRA team calls etc). Provides trial status tracking and progress update...Remote job
- A Franco-Saudi CRO is seeking a clinical research professional in Riyadh. The role involves monitoring clinical trial sites, ensuring GCP compliance, and collaboration with international teams. Candidates should have a valid GCP certification and a minimum of 2 years of...
- ...May provide direct supervision, training and/or mentorship to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned. May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or...
- ...the Chalhoub Retail Academy in line with the Division objectives and strategic objectives of the group Formulate and communicate CRA performance objectives and continuously monitor progress and alignment towards strategic objectives Managerial: Develop the CRA...
- ...solutions to customer challenges Understanding of or willingness to learn about regulations and industry standards such as DORA, CRA, EU AI Act, GDPR, ISO, NIS2, SAMA, SOX, and other compliance frameworks Ability to work independently with guidance as well as collaborate...
- ...with remote guidance✓ Conduct rigorous Source Data Verification (SDV) and ensure GCP compliance✓ Collaborate seamlessly with our Paris CRA team and UAE hospital sites✓ Manage site relationships professionally with minimal supervision. Responsibilities Monitor...
