Senior Data Coordinator

Job Overview:Supports validation activities as assigned and serves as a validation team member.Review to make oneself familiar with the EDC specifications.Writes and assembles validation documentation packages such as but not limited to, validation plan, testing results, traceability matrix, validation reports.Support virtual global validation team as needed to complete validation projectsMaintains and utilizes knowledge of SOPs and validation procedures/standards in relation to system development cycle.Executes test cases against requirement, enters errors in error tracking logs and performs re-test documenting resolutions.Supports in maintaining testing documentation and files.Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).Perform other duties as assigned by senior staff and/or manager.

 Education/Qualifications:University/college degree (life science, computer science, programming, pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.g., nursing certification, computer science, medical or laboratory technology)

 Basic knowledge of drug development process and Clinical Data Management System. Basic knowledge of relational databases preferredFluent in English, both written and verbalExperience:Three point five to Six (3.5-6) relevant work experience to include data management and database support:Good problem solving skills and a proactive approachGood oral and written communication skillsBasic knowledge of clinical trial process to support operations preferredAbility to work in a team environmentAbility to work effectively under supervision

 Ability to prioritize workSelf-motivatedGood time management skills and maintain the highest standards of quality work

A cooperative and team oriented approach