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Imaging Cro Jobs in Georgia (NOW HIRING)

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

... outsourced to CRO's. * Develop and maintain Data Management Plans (DMPs), CRFs, edit check ... Conduct and oversee data reconciliation, external data integrations (labs, imaging, etc.), and ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

... outsourced to CRO's. * Develop and maintain Data Management Plans (DMPs), CRFs, edit check ... Conduct and oversee data reconciliation, external data integrations (labs, imaging, etc.), and ...

Gauss Management Research & Engineering

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... night vision imaging systems lighting. * Ferry flights may be conducted under day or night ... Designated as the local Contractor's Requesting Official (CRO) and Single Point of Contact. WHY ...

Gauss Management Research & Engineering

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... night vision imaging systems lighting. * Ferry flights may be conducted under day or night ... Designated as the local Contractor's Requesting Official (CRO) and Single Point of Contact. WHY ...

GMRE

HH-60 FCF Pilot

Moody Air Force Base, GA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... night vision imaging systems lighting. * Ferry flights may be conducted under day or night ... Designated as the local Contractor's Requesting Official (CRO) and Single Point of Contact. WHY ...

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Imaging Cro information

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 the key skills and qualifications needed to thrive as an Imaging CRO professional?

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 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 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 popular job titles related to Imaging Cro jobs in Georgia?

For Imaging Cro jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Imaging Cro jobs in Georgia look for?

The top searched job categories for Imaging Cro jobs in Georgia are:

What cities in Georgia are hiring for Imaging Cro jobs?

Cities in Georgia with the most Imaging Cro job openings:

Imaging Cro jobs near you

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device

Location: Remote

Position Summary:

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

Minimum Education and/or Experience:

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role. CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  • 401(k)
  • Dental insurance
  • Vision insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account or Health Savings Account
  • Health insurance
  • Life insurance
  • Paid time off

Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%