Imaging Research Associate I
Clario
Summary
Clario, a part of Thermo Fisher Scientific, is seeking an Imaging Research Associate I to support the coordination of site and operational activities across the full lifecycle of clinical imaging studies. In this role, you will work closely with project teams, sites, and sponsors to ensure the timely delivery of high-quality study data and service deliverables. This position plays an important role in supporting compliant, efficient clinical research operations that help bring life-changing therapies to patients faster.
Job description
What You’ll Be Doing
- Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up activities and preparation of study materials.
- Follow up on required documentation to support site qualification and schedule logistical and technical training with site personnel.
- Create test-run requests for sites submitting digital data and review, process, track, and monitor study-related data received from sites.
- Monitor and resolve data discrepancies, conduct logistical edit checks, and report issues identified within study systems.
- Perform day-to-day image quality control (IQC) activities, including coordinating, requesting, tracking, and processing IQC data in accordance with standard operating procedures (SOPs) and study protocol requirements.
- Manage site communications, generate reports and queries, and verify information for accuracy before distribution.
- Communicate with clinical study teams and sponsors regarding study deliverables and maintain accurate information within the study database.
- Prepare bone mineral density (BMD) Scan Review Forms and support Project Managers with project administration, tracking, and reporting.
- Participate in project meetings, conference calls, and training sessions.
What We Look For
- High school diploma required; an Associate or Bachelor’s degree in bioscience, computer science, information technology, or a related field is preferred.
- Familiarity with PC-based computers and standard software, including Microsoft Word, Excel, email, and databases.
- Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred.
- Ability to navigate computer networks and manage electronic files effectively.
- Strong attention to detail, organization, and ability to manage changing priorities and deadlines.
- Clear verbal and written communication skills and the ability to collaborate effectively with colleagues, sites, and study teams.
- Ability to work independently while contributing effectively in a team environment.
- Professional interpersonal skills and the ability to take ownership of assigned responsibilities.
Requirements
- High school diploma required
- Associate or Bachelor’s degree in bioscience, computer science, information technology, or related field preferred
- Familiarity with PC-based computers and standard software, including Microsoft Word, Excel, email, and databases
- Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines preferred
- Ability to navigate computer networks and manage electronic files effectively
- Strong attention to detail, organization, and ability to manage changing priorities and deadlines
- Clear verbal and written communication skills and ability to collaborate effectively
- Ability to work independently while contributing effectively in a team environment
- Professional interpersonal skills and ability to take ownership of assigned responsibilities
Benefits
- Competitive compensation
- Medical, Dental & Vision
- Remote and hybrid work options
- Tuition reimbursement
- Employee assistance program
- Wellness programs
- Life and disability insurance
Company overview
Clario is a leading provider of technology solutions for clinical trials, offering comprehensive services that support pharmaceutical, biotechnology, and medical device companies throughout the drug development process. The company specializes in electronic clinical outcome assessments (eCOA), cardiac safety solutions, medical imaging services, and endpoint management. With decades of experience in the clinical research industry, Clario combines scientific expertise with advanced technology platforms to deliver reliable data collection and analysis services. Their solutions help streamline clinical trial operations, improve data quality, and accelerate drug development timelines. Clario's global presence and integrated technology ecosystem make it a trusted partner for organizations conducting complex clinical studies across various therapeutic areas, from early-phase research to post-marketing surveillance.