Officer - Medical Imaging

The primary responsibility of the Imaging Research Associate is to assist the MI team with Image quality control, Site activities from Medical Imaging Team and medical Imaging software user testing. The Imaging Research Associate interfaces with LTR-MI team at all levels, with support activities provided in areas including, but not limited to, Image Quality and query management. document change control, proposal, and document support, administering of training, inspection readiness assessments, and nonconformance file (CAPA and Deviation) management and Data Validation

The Imaging Research Associate is a QC oriented individual, facilitating timely management quality decision making. This individual is key in achieving business and stakeholder needs with respect to meet the timelines and deliverables.

RESPONSIBILITIES

Provide assistance in setting up Medical Imaging Laboratory Facility.

Assist in development of Imaging Data flow

Feasibility Assessment for imaging component of the project to identify competent Investigator s site.

Schedule and/or impart required training to the site staff on Image Acquisition procedures and requirements.

Customize the Imaging project specific documentation

Maintain the Trail master file for the assigned projects

Manage the Independent review process, Coordination with Radiologists and other required personnel.

Keep track of Imaging Studies received from the site

Perform the Quality checks on the imaging received from the site

Conduct each activity as the predefined department/organization s SOP

Any other activities that organization had given

SKILLS

Must have great attention to detail and excellent oral and written communication skills.

Ability to excel in a team environment.

Must have the ability to multitask and work under pressure.

Must have strong time management and organizational skills. Prioritizing workload to the changing needs of the day-to-day business is a critical skill

Ability to assess the importance of a phone call, email, or document and take appropriate action to involve the required parties quickly and accurately

Work precisely according to all procedures, rules, and regulations

Must maintain strict confidentiality of sensitive data, records, files, conversations, etc.

Self-motivated and able to grasp new concepts quickly

EDUCATION AND EXPERIENCE

bachelor s degree or relevant experience is preferred.

Data entry experience/competence required.

Working knowledge of medical terminology preferred

Knowledge of clinical trials and/or healthcare industries is required.

Expertise in using MS Office and internet applications required.

Accountability

Communication

Work Ethic

Initiative

Leadership

Employment History

Technical Knowledge

Academic Qualifications

Motivation/Initiative

Interpersonal / Leadership skills

Presentation / Communication skills

Impression and Enthusiasm

Organizational Culture fit

Accomplishments Strengths

Flexibility/Planning Organizing