Ref #: 29546

Employment type: Permanent - Full-Time

Location: Ireland

Posted: 21-Jun-2021

Description

As a sponsor-dedicated clinical trial manager, you will work on an exciting range of clinical trials. You will demonstrate a solid clinical study management track record across several countries and regions. You can work fully homebased in Ireland

Your main responsibilities will include the planning and management of clinical studies conducted by global development team through the leadership of the cross-functional clinical study team. You will contribute to study-level risk assessments, lead risk mitigation activities to ensure study delivery to plan as well as collaborate with the regional CTMs to ensure country level study delivery are fully aligned with global delivery plans

You will have the proven to manage study-level budget and timelines as well as lead the development and implementation of global Drug Supply Plan

What is required

• BA/BS/BSc or RN
• Previous experience of project managing international clinical studies within the clinical research industry, i.e. within pharma, CRO or biotech working environments, ideally 5 to 7 years
• Previous clinical study management/project management as a Clinical Study Manager gained in Ireland
• Experience in overseeing external clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred
• Ability to use scientific and clinical knowledge to conceptualize study designs
• Full and valid working eligibility
• Ideally able to start ASAP/negotiable

You will be rewarded with a permanent and full-time contract of employment seconded to the client. You will have the flexibility of working fully homebased. We will offer you a competitive salary with excellent company benefits



For more details, please contact me at Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

#PMjob