Clinical Project Manager, Global

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies.

The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The Global Clinical Project Manager is the main liaison between the study team and the Clinical Program Team (CPT) starting with study handover through to close-out and archiving. The Global Clinical Project Manager is accountable to the CPT for the delivery of a study according to agreed upon timelines, budget, and quality standards by ensuring an effective partnership and teamwork within study team and / or external partners.

The Global Clinical Project Manager leads the study team and / or study oversight team in accordance with the study team operating model, current clinical trial regulations (e.g. ICH GCP).

This is a permanent role with ICON on FSP and fully home-based. You must be located in the following countries to be consider : Bulgaria, UK, Poland OR Spain.

• Lead, provide guidance and delegate appropriately to a cross-functional study team or oversee outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and quality standards. May hold accountability and / or oversight of several studies
• Lead and facilitate communication across all functions, including external partners and service providers.
• Lead and conduct investigator meetings and other study related meetings.

Provide input into and hold accountability for the development of essential study level documents (i.e., Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant SOPs.

You must have current experience working in the clinical reserach industry within a Pharma or CRO setting within Global study delivery.

You must have the right to work with no sponsorship requirements in the following countries : Spain, UK, Poland and Bulgaria

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