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. 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.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.May contribute to the development of study tools and materials as well as documentation for clinical trialsMay provide mentoring, training, and co-monitoring of junior CRAs and other clinical team membersPrepare 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 staffEffectively documents observations in site visit reports and follow up letters within timelines required by Rho’s procedural documents and the applicable clinical monitoring planMay assist in payment processes, including liaison with Site and review Site and patient data for visits being invoicedFor Senior CRAs :
Provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members.May support Clinical Team Lead and Project Management tasks on assigned studies as-requested (e.G. study specific process development, trip report review, newsletter creation, leading CRA project team calls, etc.)Bachelor’s degree, preferably in a life science, nursing, pharmacy, or related science fieldRegistered Nursing certification or equivalent or relevant formal academic / vocational qualification (such as LPN) combined with a minimum of 2 years of clinical monitoring experience and demonstrated clinical monitoring knowledge may be considered in lieu of a Bachelor’s degree2 years of on-site monitoring experience within the CRO, pharmaceutical or biotechnology industryFluent in English and local languageProficient knowledge of ICH-GCP and country specific clinical monitoring guidelinesProven clinical monitoring skillsPlease submit your CV in English.J-18808-LjbffrJ-18808-Ljbffr
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