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Medical Imaging Specialist Lead

1 week ago


Hyderabad, Telangana, India Imaging Endpoints Full time

About Us:

Imaging Endpoints is a leading provider of imaging technology and services, dedicated to advancing the field of medical imaging. Our team of experts works tirelessly to connect imaging to the cure, improving the lives of cancer patients through innovative solutions.

Job Description:

We are seeking a highly skilled Clinical Trial Imaging Specialist/Clinical Trial Imaging Specialist II to join our team. As a key member of our operations department, you will be responsible for conducting quality control/analysis procedures, performing read assignments, and ensuring technical adequacy and data integrity.

Responsibilities:

  • Perform technical quality review of images per trial specifications
  • Perform Quantitative image analysis
  • Manage research projects and early phase clinical trials
  • Complete quality control documentation according to standard operating procedures
  • Develop quality control documentation in conjunction with the Project Manager
  • Generate, track, and resolve image queries
  • Identify and assign cases ready for read assignment
  • Prepare study dossiers to be associated with read assignment
  • Track the read assignment status and additional information in Clinical Trial Management Systems (CTMS)
  • Clinical site and imaging center support
  • Creation and review of imaging site questionnaires
  • Develop training materials for imaging site personnel
  • Perform technical training of imaging site personnel
  • Maintain TMF and ensure appropriate study documents are filed for audit readiness
  • Assist in the training of internal staff

Requirements:

  • Bachelor's degree in a science or health-related field or Registered Technologist (R.T.) with advance modality experience in CT, MRI, or Nuclear Medicine preferred
  • Proficiency in MS Office and internet applications required
  • Minimum of 2 years of experience in medical imaging required
  • Minimum of 1 year of experience in the clinical trials industry preferred
  • Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred
  • Knowledge of image trial documents strongly preferred

Skills:

  • Proficiency in MS Office and internet applications
  • Service-oriented approach, flexible, and proactive toward adapting to client needs
  • Ability to manage project activities with diverse groups and individuals with little supervision
  • Must have superior attention to detail including excellent oral and written communication skills
  • Must have the ability to work independently, multitask, and meet critical timelines under pressure
  • Must have strong time management and organization skills
  • Self-driven, ability to get the job done with little supervision, can-do positive attitude
  • Ability to excel in a team environment
  • Ability to work in strict compliance with all procedures, rules, and regulations
  • Maintain strict confidentiality of sensitive data, records, files, conversations, etc.