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Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials. We combine deep scientific expertise with advanced technology to deliver reliable, highquality clinical trial outcomes. We are seeking an Imaging Research Associate I to support imaging and IQC activities across global clinical studies, ensuring accuracy, compliance, and timely delivery of study milestones.What We OfferCompetitive compensation aligned to the local marketComprehensive benefits package in accordance with Costa Rica employment standardsExposure to global clinical trials and crossfunctional collaborationStructured onboarding, training, and professional development opportunities.A collaborative, qualitydriven, and inclusive work environment.What Youll Be DoingCoordinate site and operational activities from study startup through study close to support highquality study deliveryAssist with preparation and distribution of study materials and follow up on outstanding site documentationSchedule and coordinate logistical and technical trainings for clinical site personnelReview, process, track, and monitor imaging and studyrelated data received from sitesSupport identification, tracking, and resolution of data discrepancies and logistical edit checksPerform daytoday Imaging Quality Control (IQC) activities, including baseline, interim, and endofstudy IQC data reviewCoordinate phantom rotations, analyze phantom data, and ensure accurate data entry and trackingSupport machine change documentation, equivalence data collection, and machine equivalence analysisMaintain study databases and tracking systems, ensuring data accuracy and compliance with SOPs and protocolsGenerate, review, and distribute site, patient, and project tracking reportsCommunicate with internal study teams, sites, and sponsors regarding deliverables and timelinesAssist Project Managers with site startup activities, project tracking, data flow monitoring, and issue resolutionParticipate in project meetings, training calls, and crossfunctional discussions.What We Look ForHigh School Diploma required; Associates or Bachelors degree in bioscience, computer science, information technology, or a related field preferredFamiliarity with PCbased systems and standard software tools (email, word processing, Excel, databases)Basic understanding of clinical trials, drug development, or pharmaceutical research preferredKnowledge of Good Clinical Practices (GCP) preferredStrong attention to detail, organizational skills, and documentation practicesAbility to work independently and collaboratively in a fastpaced, deadlinedriven environmentClear verbal and written communication skills and a professional, serviceoriented mindsetClario is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.EEO StatementBioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.Originally posted on Himalayas Apply To this Job .