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Imaging Cro information

What is the difference between Imaging Cro vs MRI Technologist?

AspectImaging CroMRI Technologist
Required CredentialsCertification in radiologic technology, ARRT certificationCertification in radiologic technology, ARRT certification with MRI specialization
Work EnvironmentHospitals, clinics, outpatient imaging centersHospitals, diagnostic imaging centers, outpatient clinics
Industry UsageUsed across various imaging modalities including MRI, CT, X-raySpecializes in MRI procedures only
Common Search/ComparisonOften compared for imaging roles requiring certification and patient careCompared for MRI-specific roles and certifications

Imaging Cro professionals typically have certifications in radiologic technology and work in diverse imaging environments, including MRI. MRI Technologists specialize specifically in MRI procedures, often requiring additional MRI-specific certification. Both roles are vital in diagnostic imaging, but Imaging Cro has a broader scope, while MRI Technologists focus solely on MRI imaging.

What are some common challenges faced by Imaging CRO professionals when managing multiple clinical studies simultaneously?

Imaging CRO professionals often juggle several clinical studies at once, which can present challenges such as coordinating timelines, ensuring consistent quality across different projects, and managing communication between sponsors, imaging sites, and internal teams. Staying organized and prioritizing tasks is crucial, as delays or errors in image data collection and analysis can impact study outcomes. Utilizing robust project management tools and maintaining clear documentation can help address these challenges, while regular team meetings foster collaboration and keep everyone aligned.

What are the key skills and qualifications needed to thrive as an Imaging CRO (Contract Research Organization) professional, and why are they important?

To thrive as an Imaging CRO professional, you need expertise in clinical imaging protocols, data management, and a background in medical imaging or related life sciences, often supported by a relevant degree. Familiarity with imaging software (such as DICOM viewers), compliance systems, and industry certifications (e.g., GCP) is typically required. Strong attention to detail, project management, and effective communication skills help manage complex clinical trials and client relationships. These skills ensure accurate imaging data collection and analysis, regulatory compliance, and successful project delivery in clinical research.

What does an Imaging CRO do?

An Imaging CRO (Contract Research Organization) specializes in providing imaging services for clinical trials and medical research. They manage the acquisition, analysis, and interpretation of medical images, such as MRI, CT, or X-ray scans, to support drug development and regulatory submissions. Imaging CROs ensure that imaging data is collected according to standardized protocols and meets regulatory requirements, helping pharmaceutical and biotech companies achieve reliable trial results. Their expertise helps improve the quality, consistency, and efficiency of imaging data in research studies.
What are popular job titles related to Imaging Cro jobs in Indiana? For Imaging Cro jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Imaging Cro jobs in Indiana look for? The top searched job categories for Imaging Cro jobs in Indiana are:
Imaging Cro jobs near you

Clinical Research Coordinator

P1 Pratia Oncology

Fort Wayne, IN • On-site

$22.25 - $29.50/hr

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

P1 Pratia Oncology (formerly P1 Trials) is a network of world-class, community-based oncology investigative sites capable of performing complex Phase 1 clinical trials. We emphasize standardization and centralization of clinical trial operations to ensure efficiency, high-quality data, and faster study start-up timelines. With a patient-centric approach and collaboration with our pharmaceutical, biotech, and CRO partners, we are dedicated to delivering reliable outcomes that support groundbreaking medical advancements. As our team continues to grow in the US, we are hiring a clinical research coordinator who will support the safe, compliant, and efficient conduct of early-phase oncology clinical trials across the P1 Pratia Network.


As a Clinical Research Coordinator, you will:


  • Assist with daily clinical trial activities from study start-up through close-out.
  • Schedule and facilitate study visits, assessments, and follow-up appointments.
  • Support investigational product accountability when delegated.
  • Track and document protocol deviations; support corrective actions.
  • Assist with site qualification, initiation, monitoring, and close-out visits.
  • Conduct pre-screening and confirm eligibility according to protocol criteria.
  • Coordinate labs, imaging, procedures, and specialist referrals.
  • Document protocol compliance, including investigational product adherence.
  • Maintain essential regulatory documents per ICH-GCP, FDA, and institutional standards.
  • Support IRB submissions, amendments, safety reports, and renewals.
  • Maintain delegation logs and protocol version control.
  • Promote adherence to SOPs and process improvement initiatives.
  • Enter and verify data in EDC systems within sponsor timelines.
  • Resolve data queries promptly and collaborate with monitors.
  • Oversee completion of case report forms (CRFs).
  • Assist with audits and inspections.
  • Coordinate with Pharmacy for IP accountability and dispensing when delegated.
  • Coordinate with Laboratory for specimen processing and shipping.
  • Coordinate with Radiology for protocol-window imaging.
  • Document and follow up on adverse events (AEs) and serious adverse events (SAEs).
  • Report safety events per protocol and regulatory timelines.
  • Assist with feasibility, qualification, and study start-up activities.
  • Track study visit completion and billable items.


Knowledge, Skills and Abilities

  • Working knowledge of ICH-GCP and FDA regulations
  • Attention to detail and accuracy in documentation, data entry, and regulatory records.
  • Proficiency with clinical trial systems (e.g., EDC, CTMS) and standard office software.


Requirements

  • High school diploma or GED
  • Prior experience as a CRC or equivalent clinical research role (oncology preferred).


The anticipated salary range for this role is 65-80k/yearly. Actual compensation will depend on experience, location, and other factors.


Candidates must be authorized to work in the United States without current or future sponsorship.

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