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Job Description & How to Apply Below
Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts;
London, UK;
Leiden, Netherlands;
Basel, Switzerland;
Hyderabad, India and Shanghai, China. We are an affiliate of Honor Health, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/Rad Partners), the largest private radiology group in the United States. We are recognized as the world’s largest and most preeminent iCRO in oncology.
Under the direction of Imaging Operations Leadership, the Clinical Database Developer is primarily responsible for configuring and administrating Imaging Endpoints Clinical Trial Management System (iCTMS) and other clinical database systems as directed. This role will coordinate with the iCTMS vendor and iCTMS team members. The CDD will manage report development and system enhancements.
CLINICAL DATABASE DEVELOPER
RESPONSIBILITIES
Collaborate with Project Management, Operations, and Data management to define system specifications, workflow, and documentation practices
Lead project management activity related to the deployment of iCTMS, and other clinical database systems
Analyze complex electronic case report form requests to determine feasibility for incorporation within clinical studies
Support and/or lead data reporting activities by gathering user requirements, developing report specifications, and implementing both standardized and ad-hoc reports
Engage with software vendors to understand their roadmaps and communicating functionality requirements of Imaging Endpoints
Assist in user administration and operational support, including user and security management
Assist in the creation of necessary training materials and SOPs related to clinical database systems
Assist in the training of internal and external staff (when needed)
Assist with the implementation and validation of a new imaging iCTMS as well as the migration of current studies to the new solution
Assist in building, maintaining, and deploying study databases to collect clinical trial data, including custom system configurations and integrations
Monitor and assist other iCTMS team members with the study build and new improvements
Other duties as assigned by the manager
EDUCATION AND EXPERIENCE
Bachelor’s degree in life sciences, computer science or equivalent work experience required
Minimum of 3 years of experience developing data collection modules within EDC or other clinical database systems is required
Knowledge and understanding of clinical development, FDA regulations, and Good Clinical
Practices
Proficiency in understanding software programming code, especially SQL dataset operations involving complex joins and record mergers
Experience with relational data modeling techniques
Experience with enterprise reporting applications preferred
Must have:
2–5 years’ hands‑on EDC build experience (Clindex preferred; Medidata Rave, Oracle InForm, Veeva, Medrio, Open Clinica accepted)
Experience configuring CRFs/edit checks/visit schedules/user roles, practical test planning/UAT
Basic SQL
Nice-to-have:
Clindex experience and CDISC SDTM/data-standards mapping experience.
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 group 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…
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