Imaging Research Associate I

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, high‑quality 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 Offer

• Competitive compensation aligned to the local market

• Comprehensive benefits package in accordance with Costa Rica employment standards

• Exposure to global clinical trials and cross‑functional collaboration

• Structured onboarding, training, and professional development opportunities

• .A collaborative, quality‑driven, and inclusive work environment.
   

What You’ll Be Doing

• Coordinate site and operational activities from study start‑up through study close to support high‑quality study delivery

• Assist with preparation and distribution of study materials and follow up on outstanding site documentation

• Schedule and coordinate logistical and technical trainings for clinical site personnel

• Review, process, track, and monitor imaging and study‑related data received from sites

• Support identification, tracking, and resolution of data discrepancies and logistical edit checks

• Perform day‑to‑day Imaging Quality Control (IQC) activities, including baseline, interim, and end‑of‑study IQC data review

• Coordinate phantom rotations, analyze phantom data, and ensure accurate data entry and tracking

• Support machine change documentation, equivalence data collection, and machine equivalence analysis

• Maintain study databases and tracking systems, ensuring data accuracy and compliance with SOPs and protocols

• Generate, review, and distribute site, patient, and project tracking reports

• Communicate with internal study teams, sites, and sponsors regarding deliverables and timelines

• Assist Project Managers with site start‑up activities, project tracking, data flow monitoring, and issue resolution

• Participate in project meetings, training calls, and cross‑functional discussions.
   

What We Look For

• High School Diploma required; Associate’s or Bachelor’s degree in bioscience, computer science, information technology, or a related field preferred

• Familiarity with PC‑based systems and standard software tools (email, word processing, Excel, databases)

• Basic understanding of clinical trials, drug development, or pharmaceutical research preferred

• Knowledge of Good Clinical Practices (GCP) preferred

• Strong attention to detail, organizational skills, and documentation practices

• Ability to work independently and collaboratively in a fast‑paced, deadline‑driven environment

• Clear verbal and written communication skills and a professional, service‑oriented mindset
   

Clario is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

EEO Statement

Bioclinica 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.