Our client is a privately owned Biotech company who specialise in the development of innovative drugs. Due to continued success, they seek to hire an experienced Clinical Study Manager to join their team on a permanent basis.

The Role:

The main objectives for the role will include:

• Project Management for the set up and conduct of clinical trials.
• Participate in CRO and other third-party vendor selection, management including review of contracts and budget.
• Act as the line of communication to relevant stakeholders and provides input to project progress and reporting.
• Document preparation, tracking timelines, budget, and quality metrics.
• Contributes to the revision of Standard Operating Procedures, guidelines, and departmental policies.

The Person:

In order to be considered you must have the following:

• A third level degree in Science, Healthcare or related.
• 3-5+ years' experience as a Clinicall Study Manager.
• Experience in managing multi-site clinical studies, preferably global.
• Understanding of Global and EU legal requirements and GCP.
• Ability to work autonomously.
• Eligibility to live and work in the EU.

To discover more about this opportunity, apply now or contact Gillian McMurrough at HRM on +353 87241 4486 for a confidential discussion.