Senior Clinical Developer

Description

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.

Responsibilities:

• 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.
• Oversee 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 requirements and convert them to reports.
• 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 in related 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.