[Remote] Scientist- MRI (Imaging Clinical Research)
Note: The job is a remote job and is open to candidates in USA. Perceptive Inc. is seeking a Scientist specializing in MRI for clinical research projects. The role involves providing scientific input on clinical trials, developing imaging guidelines, and conducting training for project teams and reviewers.
Responsibilities
ā¢ Independently author internal and external facing documents and material such as: Standardized/Harmonized imaging parameters ā Image Acquisition Guidelines (e.g., develop imaging parameters for specific clinical protocols to ensure standardization of imaging techniques in multi-center trials)
ā¢ With supervision ā Review and provide input to relevant project related documents such as: Project Plan, Site Operations Manual, if requested, Independent Review Charter, Image QC and processing instructions (QC Form), Reviewer Manual, if applicable, Clinical Data Transfer Instructions, if applicable
ā¢ With supervision: Create training material for and present to investigator sites, CRA and client (as needed) such as PowerPoint presentation, site guides on assessment criteria and imaging parameters
ā¢ With supervision: Create training material for and present to internal team on image acquisition parameters, quality control and image processing, e.g. image operations
ā¢ With supervision: Review requirement specifications of analysis application (including eCRF) and associated applications, and customization of relevant image viewing/analysis tools
ā¢ With supervision: Conduct User Acceptance Testing
ā¢ Review CVs of potential independent reviewers
ā¢ With supervision - prepare and conduct Independent Reviewer Trainings, including: Prepare Independent reviewer Training PowerPoint slides, Review/Edit training associated documentation, Select/Prepare training and testing cases for reviewer training, Lead training of independent reviewers on the use of imaging software, analysis applications, and implementation of the review criteria
ā¢ With supervision perform quality control and evaluation of the results of the independent review and provide necessary guidance and feedback to independent reviewers
ā¢ Identify non-compliances and non-conformances
ā¢ Review audit findings, determine the risks associated with those findings and ensure that corrective actions are carried out
ā¢ Participate in project related client meetings
ā¢ Effective and professional communication with internal and external stakeholders; act as a translator as needed
ā¢ Identify, evaluate and communicate potential risks related to deliverables as well as their mitigation
ā¢ Actively maintain and disseminate knowledge in one or more identifiable specialisms
Skills
ā¢ Provide scientific input on projects for clinical trials where medical imaging and clinical data is used to evaluate efficacy and/or safety of investigational drugs or medical devices
ā¢ Work with the project team lead on project related aspects of documents, application development with supervision
ā¢ Lead the development of image acquisition guidelines, medical documentation, preparation and conduct of external project team training, central reviewer training and reviewer quality control from a medical / scientific perspective in consultation with the relevant internal support and stakeholders
ā¢ Independently author internal and external facing documents and material such as Standardized/Harmonized imaging parameters ā Image Acquisition Guidelines
ā¢ Review and provide input to relevant project related documents such as Project Plan, Site Operations Manual, Independent Review Charter, Image QC and processing instructions, Reviewer Manual, Clinical Data Transfer Instructions
ā¢ Create training material for and present to investigator sites, CRA and client
ā¢ Review requirement specifications of analysis application and associated applications, and customization of relevant image viewing/analysis tools
ā¢ Conduct User Acceptance Testing
ā¢ Review CVs of potential independent reviewers
ā¢ Prepare and conduct Independent Reviewer Trainings
ā¢ Perform quality control and evaluation of the results of the independent review and provide necessary guidance and feedback to independent reviewers
ā¢ Identify non-compliances and non-conformances
ā¢ Review audit findings, determine the risks associated with those findings and ensure that corrective actions are carried out
ā¢ Participate in project related client meetings
ā¢ Effective and professional communication with internal and external stakeholders
ā¢ Identify, evaluate and communicate potential risks related to deliverables as well as their mitigation
ā¢ Actively maintain and disseminate knowledge in one or more identifiable specialisms
ā¢ Demonstrable ability to design and deliver training to a varied and global audience at all levels
ā¢ Demonstrable knowledge of medical terminology and practices
ā¢ Proven understanding of research methodologies and pragmatic application in a regulated environment
ā¢ Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
ā¢ Excellent interpersonal, verbal and written communication skills
ā¢ A flexible attitude with respect to work assignments and new learning
ā¢ Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
ā¢ Ability to work methodically in a fast-paced, time-sensitive environment
ā¢ Demonstratable ability to apply critical thinking to problems and tasks
ā¢ Ability to identify and implement process improvements
ā¢ Proactively participates in skills improvement training and encourages teams to participate
ā¢ Maintain an up-to-date awareness of trends, tools, technology, techniques, processes and developments within the Life sciences domain
ā¢ A self-starter and able to work under own initiative
ā¢ Experience using tools to communicate progress to Stakeholders
ā¢ Solid proven experience of working in and knowledge of medical imaging or clinical development in the life sciences industry and regulated environments
ā¢ Solid professional experience in the same or very similar role
ā¢ MS/MA, RPh with experience or BA/BS/RN/BSN/Technologist Certification with experience in imaging or clinical trials
ā¢ English: Fluent
ā¢ Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA are preferred
ā¢ US applicants must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future
ā¢ Experience as Advanced Imaging Cardiologist not only for MRI but for echo as well
ā¢ Experience with cardiac software such as Medis Suite MR, suiteHEART, etc
ā¢ Experience quantitative assessments of function, perfusion, flow, and mapping
Company Overview
ā¢ Expanding on their combined 50-year history, Perceptive provides best-in-class specialist support to global pharmaceutical, biotech, and clinical research organizations, spanning the complete R&D lifecycle, from discovery and preclinical through clinical development to post marketing. It was founded in 1996, and is headquartered in London, England, GBR, with a workforce of 1001-5000 employees. Its website is https://www.perceptive.com.
Apply Now
Apply Now
Responsibilities
ā¢ Independently author internal and external facing documents and material such as: Standardized/Harmonized imaging parameters ā Image Acquisition Guidelines (e.g., develop imaging parameters for specific clinical protocols to ensure standardization of imaging techniques in multi-center trials)
ā¢ With supervision ā Review and provide input to relevant project related documents such as: Project Plan, Site Operations Manual, if requested, Independent Review Charter, Image QC and processing instructions (QC Form), Reviewer Manual, if applicable, Clinical Data Transfer Instructions, if applicable
ā¢ With supervision: Create training material for and present to investigator sites, CRA and client (as needed) such as PowerPoint presentation, site guides on assessment criteria and imaging parameters
ā¢ With supervision: Create training material for and present to internal team on image acquisition parameters, quality control and image processing, e.g. image operations
ā¢ With supervision: Review requirement specifications of analysis application (including eCRF) and associated applications, and customization of relevant image viewing/analysis tools
ā¢ With supervision: Conduct User Acceptance Testing
ā¢ Review CVs of potential independent reviewers
ā¢ With supervision - prepare and conduct Independent Reviewer Trainings, including: Prepare Independent reviewer Training PowerPoint slides, Review/Edit training associated documentation, Select/Prepare training and testing cases for reviewer training, Lead training of independent reviewers on the use of imaging software, analysis applications, and implementation of the review criteria
ā¢ With supervision perform quality control and evaluation of the results of the independent review and provide necessary guidance and feedback to independent reviewers
ā¢ Identify non-compliances and non-conformances
ā¢ Review audit findings, determine the risks associated with those findings and ensure that corrective actions are carried out
ā¢ Participate in project related client meetings
ā¢ Effective and professional communication with internal and external stakeholders; act as a translator as needed
ā¢ Identify, evaluate and communicate potential risks related to deliverables as well as their mitigation
ā¢ Actively maintain and disseminate knowledge in one or more identifiable specialisms
Skills
ā¢ Provide scientific input on projects for clinical trials where medical imaging and clinical data is used to evaluate efficacy and/or safety of investigational drugs or medical devices
ā¢ Work with the project team lead on project related aspects of documents, application development with supervision
ā¢ Lead the development of image acquisition guidelines, medical documentation, preparation and conduct of external project team training, central reviewer training and reviewer quality control from a medical / scientific perspective in consultation with the relevant internal support and stakeholders
ā¢ Independently author internal and external facing documents and material such as Standardized/Harmonized imaging parameters ā Image Acquisition Guidelines
ā¢ Review and provide input to relevant project related documents such as Project Plan, Site Operations Manual, Independent Review Charter, Image QC and processing instructions, Reviewer Manual, Clinical Data Transfer Instructions
ā¢ Create training material for and present to investigator sites, CRA and client
ā¢ Review requirement specifications of analysis application and associated applications, and customization of relevant image viewing/analysis tools
ā¢ Conduct User Acceptance Testing
ā¢ Review CVs of potential independent reviewers
ā¢ Prepare and conduct Independent Reviewer Trainings
ā¢ Perform quality control and evaluation of the results of the independent review and provide necessary guidance and feedback to independent reviewers
ā¢ Identify non-compliances and non-conformances
ā¢ Review audit findings, determine the risks associated with those findings and ensure that corrective actions are carried out
ā¢ Participate in project related client meetings
ā¢ Effective and professional communication with internal and external stakeholders
ā¢ Identify, evaluate and communicate potential risks related to deliverables as well as their mitigation
ā¢ Actively maintain and disseminate knowledge in one or more identifiable specialisms
ā¢ Demonstrable ability to design and deliver training to a varied and global audience at all levels
ā¢ Demonstrable knowledge of medical terminology and practices
ā¢ Proven understanding of research methodologies and pragmatic application in a regulated environment
ā¢ Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
ā¢ Excellent interpersonal, verbal and written communication skills
ā¢ A flexible attitude with respect to work assignments and new learning
ā¢ Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
ā¢ Ability to work methodically in a fast-paced, time-sensitive environment
ā¢ Demonstratable ability to apply critical thinking to problems and tasks
ā¢ Ability to identify and implement process improvements
ā¢ Proactively participates in skills improvement training and encourages teams to participate
ā¢ Maintain an up-to-date awareness of trends, tools, technology, techniques, processes and developments within the Life sciences domain
ā¢ A self-starter and able to work under own initiative
ā¢ Experience using tools to communicate progress to Stakeholders
ā¢ Solid proven experience of working in and knowledge of medical imaging or clinical development in the life sciences industry and regulated environments
ā¢ Solid professional experience in the same or very similar role
ā¢ MS/MA, RPh with experience or BA/BS/RN/BSN/Technologist Certification with experience in imaging or clinical trials
ā¢ English: Fluent
ā¢ Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA are preferred
ā¢ US applicants must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future
ā¢ Experience as Advanced Imaging Cardiologist not only for MRI but for echo as well
ā¢ Experience with cardiac software such as Medis Suite MR, suiteHEART, etc
ā¢ Experience quantitative assessments of function, perfusion, flow, and mapping
Company Overview
ā¢ Expanding on their combined 50-year history, Perceptive provides best-in-class specialist support to global pharmaceutical, biotech, and clinical research organizations, spanning the complete R&D lifecycle, from discovery and preclinical through clinical development to post marketing. It was founded in 1996, and is headquartered in London, England, GBR, with a workforce of 1001-5000 employees. Its website is https://www.perceptive.com.
Apply Now
Apply Now