Clinical Research Associate - Usa Relocation, Valencia

Clinical Research Associate (CRA)– USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations teamsupporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company.Location: United States Visa&relocation support included Long-term assignment (2–3 years) What are we looking for? Minimum 4 years of experience as a CRA in clinical trial monitoring Strong experience performing:

La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes. - Site Selection Visits (SSV)

- Site Initiation Visits (SIV)

- Routine Monitoring Visits (RMV)

- Close-Out Visits (COV) Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes Experience managing investigative sites independently and ensuring protocol compliance Ability to work in dynamic, fast-paced, and international environments Strong communication, organizational, and stakeholder management skillsPrevious exposure to multicountry/global clinical trials is highly valued Fluent English level required Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include:Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements Conducting site qualification, initiation, routine monitoring, and close-out visits Building strong relationships with investigators, coordinators, and site staff Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycleReviewing source documentation, identifying protocol deviations, and supporting issue resolution Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams Supporting site activation, enrollment, and retention strategies Maintaining accurate and timely study documentation and monitoring reportsParticipating in investigator meetings, trainings, and study planning activities Why join CROVELIS? xiphteb CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine:International relocation to the US Career growth within global clinical operations Exposure to complex and high-visibility studies Multicultural and collaborative environment Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.