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Imaging Research Associate Jobs in Atlanta, GA (NOW HIRING)

Emory University

Abdominal Imaging Fellowship

Atlanta, GA · On-site

$307K - $384K/yr

Discover Your Career at Emory University Emory University is a leading research university that ... associates. * Demonstration of a commitment to carrying out professional responsibilities ...

Siemens Healthineers

Velocity Sales Associate

Atlanta, GA · Remote

$13.50 - $18.25/hr

... imaging centers). Who you'll work with: Work directly with Regional Vice President of Sales and ... research, compiling product communication material, leveraging internal Siemens Healthineers ...

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How much do imaging research associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for imaging research associate in Atlanta, GA is $31.66, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $36.01 per hour, depending on experience, location, and employer.

What is an imaging research associate?

Imaging Research Associates are professionals who support and conduct research studies involving medical imaging technologies, such as MRI, CT, or PET scans. They typically help design experiments, acquire and analyze imaging data, and ensure studies comply with regulatory and ethical standards. Their work is essential in advancing our understanding of diseases and developing new diagnostic or therapeutic techniques. Imaging Research Associates often collaborate closely with scientists, clinicians, and technical staff in research institutions or healthcare settings.

What are the key skills and qualifications needed to thrive as an imaging research associate?

To thrive as an Imaging Research Associate, a strong background in biomedical sciences, experience with imaging modalities (such as MRI, CT, or PET), and a relevant bachelor's or master's degree are essential. Familiarity with specialized imaging software, data analysis tools, and adherence to research protocols and regulatory requirements are typically required. Excellent analytical skills, attention to detail, and effective communication are vital soft skills for managing complex datasets and collaborating with multidisciplinary teams. These skills ensure accurate data collection, reliable research outcomes, and successful project execution in imaging studies.

What are some common challenges imaging research associates face when managing multiple imaging studies simultaneously?

Imaging Research Associates often juggle several studies at once, which can present challenges in prioritizing tasks, maintaining data accuracy, and adhering to strict study protocols. Balancing the coordination of patient appointments, quality control of imaging data, and timely communication with principal investigators requires excellent organizational skills and attention to detail. Collaborating with radiologists, technicians, and research coordinators is vital to ensure studies run smoothly and meet regulatory standards. Developing effective time management strategies and leveraging digital tools can help overcome these challenges.

What are the most commonly searched types of Imaging Research jobs in Atlanta, GA?

The most popular types of Imaging Research jobs in Atlanta, GA are:

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For Imaging Research Associate jobs in Atlanta, GA, the most frequently searched job titles are:

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The top searched job categories for Imaging Research Associate jobs in Atlanta, GA are:

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Cities near Atlanta, GA with the most Imaging Research Associate job openings:

Imaging Research Associate 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 8 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%

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