Clinical Project Manager - Slovakia

Description
Working fully outsourced to and based at the offices of a global pharma, the Clinical Project Manager is responsible for the overall successful delivery of oncology studies. Coordinating CRAs, the Clinical Project Manager ensures that study deliverables are met at a country level.

You will be instrumental in the implementation, delivery and reporting of clinical research projects, ensuring they happen on time and to budget, anticipate potential issues and actively implement preventative action plans. Typical tasks will include coordination of the CRA team, lead study start up at a country level (preparing regulatory / Health Authority submissions), budgeting and payments, participation in co-monitoring visits and review of the monitoring reports. You will track study progress and ensure compliance to ICH GCP, study protocol and SOPs.

This role is office based in Bratislava, with some flexibility for home based work.

To be considered for this position, candidates must have a proven track record within study management, including clinical team coordination from either a pharmaceutical company or a CRO environment. You will also be able to demonstrate strong leadership and problem solving skills. A strong background in oncology is highly desirable.

It is essential that you have prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements. Fluency in Slovak and English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively.