Imaging Research Associate I

eResearch Technology Inc; United States; Hybrid; USD 50,000 - 70,000; Full time

Benefits offered by this job

Competitive pay

Health insurance

Remote & Hybrid

Tuition reimbursement

Wellness programs

Life and disability insurance

Job summary

Clario is seeking an Imaging Research Associate I to coordinate site and operational activities across the full lifecycle of clinical imaging studies. You will work with project teams, sites, and sponsors to ensure timely delivery of high-quality study data and services.

In this role, you will support compliant, efficient clinical research operations and maintain accurate information within study databases. Strong attention to detail and collaboration skills are essential.

Qualifications

• High school diploma required.
• Associate or Bachelor’s degree preferred (bioscience, IT, or related).
• Familiarity with PC-based computers and Microsoft Office (Word/Excel).
• Knowledge of clinical trial processes and GCP guidelines preferred.
• Ability to navigate computer networks and manage electronic files.

Responsibilities

• Coordinate site and operational activities across the clinical imaging study lifecycle.
• Follow up on required documentation to support site qualification and schedule training.
• Create test-run requests and review data from sites.
• Monitor and resolve data discrepancies and perform IQC data processing.
• Manage site communications, generate reports, and verify accuracy before distribution.
• Communicate with clinical study teams and sponsors regarding deliverables.
• Prepare BMD Scan Review Forms and support project administration, tracking, and reporting.
• Participate in project meetings, calls, and training sessions.

Skills

Attention to detail

Communication skills

Team collaboration

Independent work

Education

High school diploma

Associate degree

Bachelor’s degree

Tools

MS Word

MS Excel

Email

Databases

Job description

What We Offer

• Competitive compensation
• Medical, dental, and vision coverage
• Remote and hybrid work options
• Tuition reimbursement
• Employee assistance and wellness programs
• Life and disability insurance

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.

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.

At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario, a part of Thermo Fisher Scientific is an equal opportunity employer.

We celebrate diversity and are committed to creating an inclusive environment for all employees.

All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Clario Privacy Policy

Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.