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Develop training materials for sponsors, site staff, and internal employees in a virtual training environment. Focus on one therapeutic area per study and provide backup for training delivery. Requires Bachelor's degree and 1+ years of corporate training experience.

The Instructional Designer is responsible for developing and maintaining role-based curriculum through various training programs like eLearning, web-based, and instructor-led courses. They work closely with subject matter experts, project teams, and clients to design and deliver technical product training courses for customers. The role involves needs analysis, content development, and managing training content repositories.

Join Clario's enterprise, centralized Data & Analytics team as a Lead Software Engineer to create and enhance data analytic products for our Life Science industry customers. Responsibilities include software design, development, support, technical expertise to senior leadership, training and supervision of junior staff, troubleshooting, code development, planning, quality assurance, and mentorship. Skills required include Full Stack Engineering, Project Management, Data Analytics, Source Code Management, Agile Development, and more.

Responsible for directing and managing services for client projects to ensure high quality, on-time, and on-budget services with a focus on customer service. Lead project planning, monitoring, and closeout phases, manage study timelines and finances, and promote collaboration within teams. Additional responsibilities include compliance, training, and assisting in various project management tasks. Requires Bachelor's degree and 1-4 years of project management experience in the pharmaceutical field, with emphasis on eCOA or related industry products.

As a Systems Analyst II at Clario, you will be responsible for creating, maintaining, and testing code for non-standard data file creation and CDISC SDTM datasets. You will also mentor junior staff, attend client meetings, develop and validate programs, create submission-ready datasets for eCOA trials, and collaborate with cross-functional teams for project delivery. This role requires a Bachelor's or Master's degree in Informatics, Mathematics, or Computer Science, along with SAS programming experience in a Pharmaceutical company or CRO.

The Senior Software Engineer will provide software design, development, and application support for a clinical trial endpoint technology company's Trial Application Platform (TAP). They will work on new and existing feature development, write testable code, collaborate with cross-functional teams, and continuously improve code and product quality.

Ensure compliance with medical device regulations, manage quality control processes, and support design projects in a manufacturing environment at Clario. Responsible for documentation, risk management, quality assurance, and regulatory compliance throughout the product life cycle.