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Rho, an award-winning, stable, full-service CRO known for its collaborative, dynamic culture based in the US, is quickly expanding their presence in Europe. We are a thriving company, and we will deliver global full-service clinical development services and unmatched customer support – worldwide. Join us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges. At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. As a Clinical Research Associate II / Sr. CRA, you will be a key player in our innovative team, dedicated to ensuring that our clinical trials are conducted with the utmost integrity and quality. Your expertise will help us navigate the complexities of clinical research as we strive to deliver meaningful solutions to healthcare challenges. The Clinical Monitoring team at Rho is known for its collaborative spirit and commitment to excellence. Join us to not only advance your career but also contribute to a culture that celebrates innovation, supports professional growth, and values every team member's input. This is a permanent CRA II / Senior CRA role to be home based role in Spain. Responsibilities: May contribute to the development of study tools and materials as well as documentation for clinical trials May provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members May provide support to the RFP process Prepare and perform all onsite & off-site/remote site monitoring visit activities across multiple protocols, inclusive of all study visit types as needed (SQV, SIV, IMV and COV), according to Good Clinical Practice(GCP), Protocol, applicable regulations and Sponsor requirements under supervision of experienced staff Effectively documents observations in site visit reports and follow up letters within timelines required by Rho's procedural documents and the applicable clinical monitoring plan Prepare (if needed) and maintain Investigator Site Files (ISF), and maintain site binders and documents of the TMF (Trial Master May assist in
