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Medical Imaging Cro Jobs (NOW HIRING)

Medpace, Inc.

Medical Imaging Analyst

Cincinnati, OH · On-site

Perform quality assurance checks on medical imaging data collected during medical and device ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...

Medpace, Inc.

Medical Imaging Analyst

Cincinnati, OH · Hybrid

Perform quality assurance checks on medical imaging data collected during medical and device ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...

Medpace, Inc.

Medical Imaging Analyst

Denver, CO · On-site

$60K - $120K/yr

Perform quality assurance checks on medical imaging data collected during medical and device ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...

Medpace, Inc.

Medical Imaging Analyst

Denver, CO · Hybrid

$60K - $120K/yr

Perform quality assurance checks on medical imaging data collected during medical and device ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We ...

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Medical Imaging Cro information

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$15

$24

$33

How much do medical imaging cro jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for medical imaging cro in the United States is $24.54, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $33.41 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Imaging CRO, and why are they important?

To thrive as a Medical Imaging Clinical Research Organization (CRO) professional, you need a strong background in medical imaging modalities, clinical trial processes, and regulatory compliance, often supported by a degree in life sciences or related fields. Familiarity with imaging software (such as PACS and DICOM), clinical trial management systems (CTMS), and certifications like ACR or ICH-GCP are typically required. Excellent attention to detail, strong project management, and effective communication skills help ensure high-quality outcomes and smooth collaboration across multidisciplinary teams. These skills and qualities are crucial for delivering accurate imaging data, maintaining regulatory standards, and supporting successful clinical research outcomes.

What is the difference between Medical Imaging Cro vs Medical Imaging Technologist?

AspectMedical Imaging CroMedical Imaging Technologist
CredentialsCertification in radiology or imaging management, often with CRO-specific trainingCertification in radiologic technology, such as ARRT or equivalent
Work EnvironmentClinical settings, hospitals, imaging centers, and sometimes remote project managementHospitals, clinics, diagnostic imaging centers
Employer & IndustryPharmaceutical companies, CROs, clinical trial organizationsHealthcare providers, hospitals, diagnostic labs
Job FocusManaging imaging services for clinical trials, coordinating imaging data collectionPerforming imaging procedures, capturing diagnostic images

While both roles involve medical imaging, a Medical Imaging CRO focuses on managing imaging processes within clinical trials and works closely with pharmaceutical companies, whereas a Medical Imaging Technologist performs diagnostic imaging procedures directly on patients in healthcare settings.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Clinical Research Director or Vice President of Clinical Operations tend to have the highest salaries, often exceeding six figures annually. These positions require extensive experience, leadership skills, and often advanced degrees or certifications like RAC or CCRP.

Is clinical research in high demand?

Clinical research is in high demand across the healthcare industry, with medical imaging professionals such as radiologists and imaging specialists often involved in research studies. The growing need for advanced imaging technologies and regulatory requirements drives employment opportunities in this field, especially for those with strong technical skills and certifications in imaging modalities.

What is the highest paid medical imaging job?

The highest paid medical imaging jobs are typically specialized roles such as radiologists, who interpret medical images and often hold medical degrees and extensive training. Radiologists can earn high salaries due to their advanced expertise, with some earning over $400,000 annually, especially with subspecialty certifications and experience.

What is a Medical Imaging CRO?

A Medical Imaging CRO (Contract Research Organization) is a specialized company that provides medical imaging services to support clinical trials and research studies for pharmaceutical, biotechnology, and medical device companies. These organizations manage imaging data, perform image analysis, and ensure compliance with regulatory standards throughout the clinical trial process. By offering their expertise, Medical Imaging CROs help sponsors ensure the accuracy, quality, and consistency of imaging data, which is crucial for evaluating the safety and efficacy of medical products.

What is an imaging cro?

An imaging CRO (Contract Research Organization) specializes in managing and conducting clinical trials related to medical imaging technologies, such as MRI, CT, or ultrasound. These organizations support pharmaceutical and medical device companies by providing expertise in imaging data collection, analysis, and regulatory compliance during drug or device development.

What are some common challenges faced by Medical Imaging CRO professionals when managing multi-site clinical trials?

Medical Imaging CRO professionals often encounter challenges such as ensuring consistent imaging protocols across multiple sites, maintaining high-quality data, and adhering to strict regulatory requirements. Coordinating with various site staff and imaging facilities requires strong communication and organizational skills. Additionally, professionals in this role must stay updated on evolving imaging technologies and regulatory standards to ensure trial integrity and compliance.
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Medical Imaging Cro jobs near you
Infographic showing various Medical Imaging Cro job openings in the United States as of July 2026, with employment types broken down into 9% Locum Tenens, 84% Full Time, 3% Part Time, 2% Contract, and 2% Summer. Highlights an 75% Physical, 3% Hybrid, and 22% Remote job distribution, with an average salary of $51,052 per year, or $24.5 per hour.
Project Manager Clinical Trials

Project Manager Clinical Trials

VIDA Diagnostics

Coralville, IA

Full-time

Posted 23 days ago

Job description

VIDA Diagnostics is a leading medical imaging CRO providing central imaging services for global clinical trials across oncology, pulmonology, cardiology, neurology, and other therapeutic areas. Our imaging experts partner with sponsors and CROs to define, execute, and deliver imaging endpoints that accelerate drug and device development.

The Project Manager, Clinical Trials, serves as the primary client-facing leader for a portfolio of 4–8 concurrent imaging studies. This role owns end-to-end project delivery—from imaging charter development and site qualification through data delivery and study close-out—while coordinating cross-functional teams internally and managing all sponsor and CRO relationships.

Responsibilities:

Study Leadership & Sponsor Management

  • Serve as the primary point of contact for sponsors and CROs for all project-specific matters throughout the study lifecycle.
  • Lead imaging study start-up, including development of the imaging charter, imaging endpoint definitions, KPIs, communication plan, and risk management plan.
  • Ensure study deliverables are provided to Sponsor/CRO on schedule with high quality.
  • Manage study maintenance and close-out activities, ensuring all deliverables are completed on time and to quality standards.
  • Assess and communicate the impact of scope changes; lead change order process and obtain sponsor approval.

Imaging Operations

  • Coordinate imaging site qualification process with Sponsor/CRO, ensuring review of site imaging equipment requirements against protocol requirements
  • Monitor imaging site training and ongoing compliance with imaging protocols, escalating site deviations and coordinating corrective actions with Sponsor/CRO
  • Monitor DICOM data receipt, analysis, reconciliation, and escalation workflows within VIDA and with third party analysis providers, providing escalation and issue resolution support when needed.

Timeline, Risk & Project Tracking

  • Develop and maintain detailed project schedules; track study progress against milestones and proactively identify risks or delays. Communicate with Sponsor/CRO study management to ensure project status is understood, and collaborate on issues resolution.
  • Own project budget tracking, both internal and with third party providers, providing regular forecast information, identification of out-of-scope activities, and oversee the preparation of change orders.
  • Report project status, metrics, and financial data to internal leadership and as input to finance for invoicing.
  • Escalate project risks with recommended mitigation strategies to Clinical Trials management, and when appropriate, the Sponsor/CRO.

Cross-Functional Coordination

  • Partner cross-functionally with imaging scientists, data management, clinical engagement, and IT/customer support to meet study objectives.
  • Facilitate internal kickoff meetings, team huddles, and sponsor calls; document action items and drive resolution.
  • Contribute to process improvement initiatives and SOP development within the Project Management function.

Qualifications

  • Bachelor’s degree in Life Sciences, Biomedical Engineering, Health Sciences, or a related field.
  • Minimum 3 years of clinical trial project management experience, preferably at a CRO or imaging CRO; sponsor-side experience also considered.
  • Working knowledge of HIPAA, Good Clinical Practice (GCP).
  • Demonstrated ability to manage multiple concurrent studies and prioritize in a fast-paced, deadline-driven environment.
  • Exceptional written and verbal communication skills, including experience presenting to sponsor stakeholders.
  • Strong attention to detail and commitment to data quality.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Project)

Preferred Qualifications

  • Direct experience with central imaging services for clinical trials, including DICOM workflows, imaging charter authorship, or imaging site qualification.
  • Familiarity with imaging modalities relevant to clinical trials (CT, MRI, PET, ultrasound) and associated acquisition parameters.
  • Knowledge of 21 CFR 812 (medical device regulations) and/or ISO 13485
  • Experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), or imaging data platforms (e.g., Medidata, Veeva Vault, IXICO, or similar).
  • Proficiency with project management or tracking platforms (e.g., Smartsheet, Asana, or equivalent).
  • PMP certification or equivalent project management credential.

All VIDA employees expected to be flexible and have an entrepreneurial mindset.  Other duties may be assigned as needed.

VIDA is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, veteran’s status, age or disability.