Clinical Data System Designer/Technical Designer at Bioforum the Data Masters

We currently have a position for a Senior Clinical Data Systems Designer (Technical designers/database architects). If you are looking fot the next step in your career and is interested in a more technical role, why not send your CV through to the Bioforum team? We are always looking for dynamic, quality driven people. 

Minimum requirements - qualifications: 

• Bachelor’s degree or above in a biomedical or science discipline and equivalent experience is required.

Minimum requirement - experience: 

• Working in a Technical designers/database architect role for at least 2-4 years.

Minimum requirement - skills: 

• Knowledge of clinical trial process flow.  Microsoft Office and EDCs knowledge is required.  (preferably RAVE or RAVEX) - 
• Basic knowledge of a programming language (eg: SQL/VBA/C# etc) will be beneficial.

Minimum requirement - competencies:

English proficiency is required

Responsibilities:

• Responsible for performing activities that follow applicable Business Practices, Standard Operating Procedures and Working Instructions and performing other duties as assigned by management.
• Oversight and/or execution of database design implementation and data validation checks programming (automated and manual) in various EDC systems in accordance with industry best practices and company/customer’s SOPs and standards as well as the management and updates surrounding any customer change requests.
• Provide support for investigation into identification of trends and troubleshooting of system related issues.
• Provide system specific support on Integrations, Custom Reporting and EDC modules.
• Perform setup of analytical reporting functionalities for study teams and/or customers.
• Assist and collaborate with Configuration specialist on system design and build considering company and/or customer standards.
• Provide support on Customer Program Level.
• Lead and/or provide support for any customer meetings as requested by the project manager.
• Collaborate with Project Managers and Configuration specialists in study related documentation e.g. Data Management Plan creation.
• Assist on data validation efforts prior to go live and as applicable during study.
• Potential hands-on study data review and/or validation including clinical database and external data reconciliation according to Project Manager guidance.
• Provide support in the development of guidance documents and associated processes for a system or specific tool.
• Knowledge of company level standards, SOPs, and processes to support reviews/updates and contribute to departmental SOP development.
• Supervise, mentor and train other Data management employees and team members.