Overview

Job description

A well-established, gradually growing international company that is currently looking for a Clinical Study Project Specialist. There are also project management tasks and responsibilities!

– Provide clinical services and achieve deadlines in accordance with roles and duties that have been established with coworkers and customers.

– Assist with information setup and upkeep in clinical trial management systems

– Constantly update information such as deadlines, milestones, EC/HA authorizations, etc.

– Assist the clinical project manager with managing the study budget by making sure that the clinical study budget is accurately planned, tracked, and reported.

– Monitor the status of clinical services and make that CTMS, TMF, and other relevant systems are up to date.

– Establishment and coordination of External Service Providers, ensuring that all necessary data, materials, and information are available for the commencement, conduct, and conclusion of the research.

Requirements

– English fluency (B2+)

– Three or more years of practical experience carrying out clinical studies for a pharmaceutical firm or contract research group

– Excellent technical and administrative abilities (Excel, MP,)

– Deep understanding of Good Clinical Practice

– Financial experience in forecasting, actuals, and cost balancing

– A track record of building productive working relationships in a multicultural and matrix setting

– Willingness to manage projects and studies responsibly

Benefits

– 5 weeks of holidays
– Sick days
– Meal vouchers
– Referral bonuses
– Multisport card
– Refreshment in the office
– Work on interesting projects
– Professional development

Note for candidate

Send us your CV in English and Czech if you have one. For more related job opportunities visit https://www.grafton.cz/en/job-search

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