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Clinical Imaging Specialist (Nuclear Medicine)

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Degree in Medical Radiation Science or equivalent, Minimum 5 years experience in medical imaging, Experience in CT, MRI or Nuclear Medicine, Minimum 1 year experience in clinical trials, Proficiency in MS Office and internet applications.

Key responsabilities:

  • Implement imaging scope in clinical trials
  • Support design of imaging requirements in research
  • Conduct technical quality reviews of images
  • Manage study-level quality control documentation
  • Perform technical training for imaging site personnel
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GenesisCare Health Care XLarge https://www.genesiscare.com/
5001 - 10000 Employees
See more GenesisCare offers

Job description

At GenesisCare we want to hear from people who are as passionate as we are about innovation and working together to drive better life outcomes for patients around the world.

Care to join our team?
GenesisCare now have an opportunity for a Clinical Imaging Specialist (Nuclear Medicine) to join our team, based in Alexandria, NSW or work remotely.

This role will be responsible for supporting central imaging and reading services to enable the development and delivery of diagnostic and therapeutic radiopharmaceutical agents to patients. The role is responsible for providing imaging expertise to deliver clinical imaging research projects through Genesis Care’s Contract Research Organisation (CRO) and Imaging Research Organisation (IRO) in Australia and internationally.

The Clinical Imaging Specialist is primarily responsible for ensuring trial data integrity and image analysis procedures. The role is responsible for reviewing the imaging data received from clinical trial sites to confirm protocol requirements have been met as well as ensuring technical adequacy and image optimisation. The role is also responsible for supporting blinded independent central reviews strategy at the IRO. This person will use their skills to initiate the evaluation of biodistributions of novel drugs with advanced image analysis techniques.

On offer is a permanent full-time position, working remotely.

More specifically, you will:

  • Implement imaging scope (calibration, central reading, dosimetry, etc) in clinical trials.
  • Support and operationalise the design of site imaging requirements in clinical research studies and associated documentations (e.g. site imaging operations manual, calibration manual, image review manual, etc).
  • Support the development and evaluation of IRO Standard Operating Procedures (SOPs), when required.
  • Support the design of technical quality review of images per trial specifications and perform these quality reviews.
  • Support the design image analysis process in conjunction with relevant stakeholders and perform quantitative image analysis when required.
  • Manage study-level quality control documentation for images according to SOPs and WIs.
  • Generate image queries to address technical issues, track those issues and ensure timely resolution.
  • Develop and maintain study-level training materials for central readers and investigator sites as well as study specific training documents.
  • Perform technical training of imaging site personnel (on-site or video-conference).

We’re interested in hearing from people who:

  • Demonstrated high level of communication and interpersonal skills in a multidisciplinary team.
  • Degree in Medical Radiation Science (or equivalent).
  • Experience in CT, MRI or Nuclear Medicine.
  • Minimum of 5 years of experience in medical imaging required.
  • Proficiency in MS Office and internet applications required.
  • Minimum of 1 year of experience in the clinical trials.
  • Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred.
  • Knowledge of image trial documents strongly preferred; i.e. Image Review Charter, Imaging Manual, Imaging Transmittal Forms, etc.
  • Prior Project Coordination duties preferred, i.e. driving timelines, deliverables and managing concurrent task.

Benefits of joining our team:

  • Own your development, learn every day and be part of GenesisCare’s rapid growth  
  • Qantas membership discount, gym membership discount, 12 weeks paid parental leave, Bupa discount.
  • The opportunity to work for one of the most influential healthcare providers.
  • Great work/ life balance with family friendly hours
  • Purchase additional annual leave as part of our annual leave scheme.
  • All employees and their family members have access to free confidential support that is completely external to GenesisCare including financial, nutritional and wellbeing coaching, legal advice & counselling.

About GenesisCare
By joining GenesisCare, you will be joining a highly progressive and passionate team of healthcare professionals and support staff, united by a common purpose: to design care experiences that deliver the best possible life outcomes. The ambition for better cancer care that began our story, has grown into a passionate team of ~2,000 employees across 50 locations nationally. Join us to design better care and enjoy a career with purpose.

Covid 19 Vaccination Requirement
In line with the Public Health Order, all GenesisCare employees are required to be fully vaccinated for COVID-19. To be eligible for consideration to perform work for GenesisCare, all recruits must provide evidence of vaccination and comply with the requirements of the Public Health Order prior to appointment.

GenesisCare is an Equal Opportunity Employer.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Health Care
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Quality Assurance
  • Microsoft Office
  • Social Skills

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