Imaging Research Associate I

OpenKrill; United States; Ibrido; USD 55.000 - 70.000; Tempo pieno

Vantaggi offerti da questo lavoro

Remote and hybrid work options

Tuition reimbursement

Medical, dental, and vision insurance

Life and disability insurance

Employee assistance programs and well‑

being wellness resources

Descrizione del lavoro

OpenKrill, on behalf of a partner company, is seeking an Imaging Research Associate I based in the United States. You will support coordination and execution of clinical imaging studies from start-up through completion, collaborating with clinical project teams, research sites, and sponsors to ensure timely, accurate data delivery and high image quality.

You will coordinate site onboarding, documentation, technical training, and the management of imaging data, contributing to study operations

Competenze

• High school diploma required; associate or bachelor’s in bioscience/CS/IT preferred.
• Familiar with PC-based systems and standard software including Word and Excel.
• Knowledge of clinical trial processes and GCP is preferred.
• Able to manage electronic files and maintain digital records.
• Strong attention to detail, multitasking, and deadline-driven.
• Good written and verbal communication with research sites and sponsors.
• Ability to work independently and within a collaborative team.
• Proactive problem-solving and commitment to quality and compliance.

Mansioni

• Coordinate site and operational activities through the imaging study lifecycle.
• Coordinate site qualification, logistics, and technical training.
• Create test-run requests and review study data from sites.
• Identify, investigate, and resolve data discrepancies and IQC data.
• Perform day-to-day image quality control activities per SOPs.
• Generate reports and queries and verify information before distribution.
• Communicate with study teams and sponsors about deliverables and databases.
• Prepare BMD Scan Review Forms and assist with project administration.
• Participate in project meetings and training sessions.

Conoscenze

Attention to detail

Communication

Independent work

Formazione

Bachelor's or Associate degree in bioscience/CS/IT

Related discipline degree preferred

Strumenti

Microsoft Word

Excel

Email platforms

Databases

Descrizione del lavoro

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for an Imaging Research Associate I based in the United States.

As an Imaging Research Associate I, you will support the coordination and execution of clinical imaging studies from start-up through completion. You will collaborate with clinical project teams, research sites, and sponsors to ensure the accurate, timely, and compliant delivery of study data. Your work will contribute to maintaining high standards of image quality and data integrity throughout the clinical research process. You will help coordinate site onboarding, documentation, technical training, and the management of imaging data. Working in a collaborative, technology-driven environment, you will contribute to efficient study operations and reliable clinical outcomes. This role offers an opportunity to develop your expertise in clinical research while supporting the advancement of innovative medical treatments. Your attention to detail and organizational skills will help accelerate the delivery of evidence that can improve patients' lives.

Accountabilities:

• Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up and the preparation of study materials.
• Follow up on documentation required for site qualification and coordinate logistical arrangements and technical training for site personnel.
• Create test-run requests for sites submitting digital data, and review, process, track, and monitor study-related data received from research sites.
• Identify, investigate, and help resolve data discrepancies, perform 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 protocols.
• Manage communications with research sites, generate reports and queries, and verify information for accuracy before distribution.
• Communicate with clinical study teams and sponsors regarding study deliverables, ensuring study databases remain accurate and up to date.
• Prepare bone mineral density (BMD) Scan Review Forms and assist Project Managers with project administration, tracking, and reporting activities.
• Participate in project meetings, conference calls, and training sessions to support effective collaboration and continuous learning.

Requirements:

• A high school diploma is required. An associate or bachelor's degree in bioscience, computer science, information technology, or a related discipline is preferred.
• Familiarity with PC-based computer systems and standard software applications, including Microsoft Word, Excel, email platforms, and databases.
• Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred.
• Ability to navigate computer networks, manage electronic files, and maintain accurate digital records.
• Strong attention to detail and organizational skills, with the ability to manage multiple tasks, adapt to changing priorities, and meet deadlines.
• Effective written and verbal communication skills, including the ability to interact professionally with research sites, colleagues, sponsors, and clinical study teams.
• Ability to work independently, take ownership of assigned responsibilities, and contribute positively to a collaborative team environment.
• Professional interpersonal skills, a proactive approach to problem-solving, and a commitment to accuracy, quality, and compliance.

Benefits:

• Competitive compensation.
• Medical, dental, and vision insurance coverage.
• Remote and hybrid work options, offering flexibility in how and where work is performed.
• Tuition reimbursement to support continued education and professional development.
• Employee assistance programs and wellness resources.
• Life and disability insurance coverage.

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