We're a proud bunch of science nerds who love tackling big challenges together. Whether you're a data wizard, analytical genius, project mastermind, or any other role, you'll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You'll have the opportunity to experience a thriving company with real stability
- financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. We are currently hiring an In-House Clinical Research Associate to join our team As an In-House CRA here at Rho, you'll have the opportunity to gain the necessary experience to grow into a traveling Clinical Research Associate (CRA) and work with the Project Manager, traveling CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed. You'll manage data entered into the CTMS (clinical trials management system) and other project tracking tools. You'll also assist CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs,
ICH/GCP guidelines, and federal regulations. Maintain the clinical trials management system (CTMS) and other project tracking tools Coordinate work with CRAs monitoring on-site Perform on site co-monitoring and remote monitoring activities Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines Bachelors Degree in a life science, nursing or pharmacy field, along with at least 1 year of direct work experience managing essential documents within the CRO, pharma or biotech industry. Good knowledge of clinical research process and an understanding of Regulatory and Central/Local ethic submission processes for assigned countries; Fluency in both local language and English. Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. Agile and Adaptable: Rho values the ability to change quickly. We embrace risk but manage it by planning, accepting, and learning from both failures and successes.
📌 In-House Clinical Research Associate (Ceuta)
🏢 Rho
📍 Ceuta