Senior Clinical Developer - ANJU
Aspire Software is looking for a Senior Clinical Developer to join our team in Lebanon.
Here is a little window into our company: Aspire Software operates and manages wholly owned software companies, providing mission-critical solutions across multiple verticals. By implementing industry best practices, Aspire delivers a time sensitive integration process, and the operation of a decentralized model has allowed it to become a hub for creating rapid growth by reinvesting in its portfolio.
- Build and maintain clinical trials for customers
- Collaborate with customers and internal resources to create accurate, complete and fully functional clinical trials.
- Document study build requirements, changes, and overall project tasks and timelines.
- Test clinical trials developed to ensure accuracy prior to moving into Quality Assurance.
- Execute mid study change requests to ensure project workflow is timely and accurate.
- Maintain study fixes for all clinical trials based on Technical Support Services escalation processes.
- Participate in Customer and Management meetings as needed.
- Oversees Clinical Development as needed to resolve technical issues.
- Troubleshoot incidents escalated to Clinical Development following Customer Care escalation processes.
- Estimate and assign project tasks to ensure workload is properly managed and distributed across the team.
- Work with stakeholders and customers to create and map requirement and convert them to report.
- Ability to identify and map data and create new reports using SQL queries.
- Develop software in compliance with industry regulations such as 21 CFR Part 11.
Requirements
- Bachelor's degree inrelated field of study or related work experience.
- Minimum of 4 + years experience with DHTML (HTML + JavaScript).
- High level understanding of SQL and IIS.
- Solid project management skills.
- Proven leadership skills.
- Knowledge of Clinical Trial Design and Setup.
- Understanding of GCP/ICH guidelines for conduction of clinical trials.
- Knowledge of FDA regulations and/or experience within the life sciences industry preferred.
- Knowledge of TrialMaster a plus