Job responsibilities

– Approve project/department specific deviations

– Coordinate internal resources and third parties/vendors for the flawless execution of projects

– Ensure that all projects are delivered on-time, within scope and within budget

– Assist in the definition of project scope and objectives, involving all relevant stakeholders and ensuring technical feasibility

– Ensure all the tasks are completed on the highest possible level of the quality

– Ensure resource availability and allocation

– Develop a detailed project plan to monitor and track progress

– Recommend changes to the project scope, project schedule and project costs using appropriate verification techniques

– Develop comprehensive project plans to be shared with clients as well as other staff members

– Manage staff performance by providing feedback, evaluation, and recognition on an ongoing basis

 

Required qualifications

– Bachelor’s degree in life sciences or computer science;
– At least 2 years data management and/or related work experience in a medical device or pharmaceutical industry/company is preferred
– Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
– Working knowledge of Clinical database applications such as EDC
– Excellent communication skills in English