Overview
Scientist role focused on supporting clinical research imaging documentation, QC, training, and related data/reporting activities.
What you'll do
- Author internal and external documents and materials for standardized/harmonized imaging parameters and guidelines.
- Review project-related documents and provide input with supervision.
- Prepare and conduct internal/external trainings related to imaging parameters, assessment criteria, and QC.
- Support application development by reviewing requirement specifications for analysis applications and customization of image tools.
- Conduct user acceptance testing and participate in independent reviewer selection, training, and performance monitoring.
- Identify non-compliances/non-conformances and help ensure corrective actions after audit findings.
- Communicate effectively with stakeholders and convey risks and mitigations related to deliverables.
What you'll need
- Experience in authoring and reviewing clinical research imaging documentation (exact years not specified).
- Ability to create and present training materials for investigator sites, CRAs, clients, and internal teams (tools like PowerPoint and guides mentioned).
- Experience with image QC/processing instructions and review documentation (QC Form, Reviewer Manual).
- Ability to review requirement specifications for analysis applications including eCRF (with supervision).
- Ability to conduct and support independent reviewer training and assess reviewer performance (with supervision).
- Strong professional communication with internal and external stakeholders (including risk communication).
Details
- Medical plan and insurance benefits are mentioned (details not quantified).
- Includes provident fund of 12% and a gratuity scheme (no amounts provided).
- Employment benefits and internal growth/training programs are mentioned.
Read the full description and apply on the company’s own careers page.
