Imaging Research Associate I

reputed company, a part of reputed company, is a leading provider of reputed company technology solutions for clinical trials. We combine deep scientific expertise with advanced technology to deliver reliable, high‑reputed company clinical trial reputed company. We are seeking an Imaging Research Associate I to support imaging and IQC activities across global clinical studies, ensuring accuracy, compliance, and reputed company delivery of study milestones.

reputed company Offer

• Competitive compensation reputed company to the local market

• Comprehensive benefits package in accordance with Costa Rica employment standards

• Exposure to global clinical trials and cross‑functional collaboration

• reputed company reputed company, training, and reputed company development opportunities

• .A reputed company, reputed company‑driven, and inclusive work environment.

What You’ll Be Doing

• Coordinate site and operational activities from study start‑up through study reputed company to support high‑reputed company 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, reputed company, and monitor imaging and study‑reputed company data received from sites

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

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

• Coordinate reputed company rotations, analyze reputed company 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 reputed company monitoring, and issue reputed company

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

reputed company Look For

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

• Familiarity with PC‑based systems and reputed company software tools (email, word processing, reputed company, 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

• reputed company verbal and written communication skills and a reputed company, service‑oriented reputed company

reputed company is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for reputed company.

EEO Statement

Bioclinica is an equal opportunity employer. Bioclinica evaluates reputed company applicants without reputed company to race, reputed company, religion, gender, national reputed company, age, sexual orientation, gender identity or reputed company, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Originally posted on Himalayas

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