Clinical Research Associate (CRA) – USA Relocation OpportunityCROVELIS 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 team supporting 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.
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Location: United StatesVisa & relocation support includedLong-term assignment (2–3 years)
What are we looking for?Minimum 4 years of experience as a CRA in clinical trial monitoringStrong experience performing:
- 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 processesExperience managing investigative sites independently and ensuring protocol complianceAbility to work in dynamic, fast-paced, and international environmentsStrong communication, organizational, and stakeholder management skillsPrevious exposure to multicountry/global clinical trials is highly valuedFluent English level required
Key ResponsibilitiesAs 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 requirementsConducting site qualification, initiation, routine monitoring, and close-out visitsBuilding strong relationships with investigators, coordinators, and site staffEnsuring patient safety, data integrity, and overall study quality throughout the trial lifecycleReviewing source documentation, identifying protocol deviations, and supporting issue resolutionCollaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teamsSupporting site activation, enrollment, and retention strategiesMaintaining accurate and timely study documentation and monitoring reportsParticipating in investigator meetings, trainings, and study planning activities
Why join CROVELIS? xhfqzwm 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 USCareer growth within global clinical operationsExposure to complex and high-visibility studiesMulticultural and collaborative environmentLong-term international experienceIf 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.