Senior Clinical Project Coordinator
hace 1 mes
We are seeking a highly skilled and experienced Associate Project Manager to join our global study team in BioPharmaceuticals Clinical Operations, Study Management.
This is a permanent role with ICON, fully home-based, and requires the candidate to be located in Hungary, Poland, Czech Republic, or Spain.
The successful candidate will lead/contribute to the preparation of delegated study documents and external service provider related documents, maintaining and facilitating interactions with internal and external functions to ensure efficient study delivery.
Key responsibilities include planning and conducting internal and external meetings, ensuring the supply of Investigational product and study materials, and proactively contributing to risk and issue identification.
The Associate Project Manager will also ensure that all study documents are complete and verified for quality in the Trial Master File, and support Global Study Directors and/or GSAD with budget management.
Requirements include a university degree, preferably in medical or biological sciences, and relevant experience from within the pharmaceutical industry or similar organization.
The ideal candidate will have excellent knowledge of international guidelines ICH/GCP, excellent communication and relationship building skills, and good project management skills.
They will also have demonstrated ability to collaborate and work independently, and demonstrated leadership skills.
Computer proficiency is also required.
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