Role & responsibilities Capable of implementing applicable procedures and associated documents. Supports team members with the fulfillment of requests from Quality Assurance. Assists team with responding to and tracking the fulfillment of general requests to Read Services. Follows general Decision Tree guidelines when liaising externally. Under general supervision, uses software tools to facilitate document collaboration. Produces clean, final legal & regulatory documents from templates and enters data accurately into designated tracking systems while maintaining data type and formatting requirements. Assists with contract preparation, onboarding, and vetting of Readers/Consultants. Under general supervision, collects manual and electronic signatures in compliance with GCP. Tracks and updates time-sensitive documentation for active Readers/Consultants. Consistently follows mandatory naming conventions and file structure requirements. Manages database and department file store to ensure audit readiness. Maintains confidentiality of project, budget, and protected health information (PHI) in strict compliance with company procedures and policies and regulatory requirements. Participates in building Reader relationships through responsive interaction with institutions, Reader vendors, and individual physicians. Contributes to process improvement initiatives. Exhibits a team approach with a positive, flexible attitude toward work assignments and learning. Preferred candidate profile Degree or equivalent work experience is required. Experience in clinical research or imaging related field preferred. Excellent verbal and written communication skills in the English language. Proficiency with using MS Office software. Strong customer orientation. Ability to work independently, effectively organize and prioritize tasks, and meet deadlines in a dynamic environment. Good problem-solving skills. Accurate and detail-oriented.
Role & responsibilities Develop and maintain data formatter repository structure. Develop data formatter for data transfer per project specific data transfer plan (DTP). Develop data processing tools for data ingestion and data export. Develop test scripts to ensure correct functionality of the developed data management tools. Document code, procedures, tests used for data QC, clinical data integration, and data transfer operations. Develop data pipelines for integration with internal and external systems. Develop Data Transfer Plans in collaboration with the Software Engineering teams. Develop in a team environment with source code management. Performs other departmental and study-related activities as needed and upon request. Preferred candidate profile Requires an advanced degree (BS or MS (preferred)) in Statistics/Biostatistics/Computer Science/Engineering or equivalent. 5+ years of STATA/SAS/Python development experience (3+ years in industry). Knowledge of Data QC (Validity, Consistency, Completeness etc.), Data Cleansing (Syntax Error Detection, Duplicate Removal, Data Auditing) & Data Transformation. Knowledge of ETL toolkits, RDBMS, No SQL DBs (desirable but not essential). Ability to work with deadlines and manage multiple priorities. Perks and benefits Best In the Industry