Imaging Research Associate I

clarioclinical; United States; Hybrid; USD 65,000 - 85,000; Full time

Benefits offered by this job

Remote work

Tuition reimbursement

Wellness programs

Life and disability insurance

Employee assistance

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, high-quality data delivery and compliant study operations.

Ideal candidates will have a strong attention to detail, knowledge of clinical trial processes, and the ability to manage changing priorities while supporting study administration and reporting.

Qualifications

• 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.

Responsibilities

• 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 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.

Skills

Data management

Documentation

Communication

Team collaboration

SOP compliance

Education

Associate or Bachelor’s degree in bioscience/IT

Tools

MS Word

MS Excel

Job description

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.

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.

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