Clinical Trial Project Manager - Ireland - Small CRO

Position: Clinical Trial Project Manager

Location: Ireland, Dublin

Reporting Into: Clinical Director

Company: Small CRO

 

Following a number of successful completed assignments, my team and I are now looking to hire a Clinical Trial Project Manager for a growing boutique CRO. Our client is positioned strategically to exciting Late Phase Designs and introducing Technology to their innovative Clinical Trials.

 

This is the perfect opportunity for a SCRA or Junior Clinical Project Manager to join a small yet growing CRO. If you are looking to make a move into Project Management, than this opportunity is perfect! Due to the company’s size & structure, you will have the opportunity to learn the ins and outs of Clinical Project Management.

 

Job Description:

 

The Clinical Trial Project Manager will:

·        Manage the technical, protocol-specific and operational aspects of assigned studies to ensure that project deliverables meet the agreed expectations.

·        Organize & provide leadership to a cross-functional team in accordance with applicable project plans, SOPs, ICH/GCP and regulatory requirements.

·        Create project management reports, plans and tools, and have the ability to implement across multiple functional groups.

·        Oversee performance of third party vendors, and have the ability to identify and implement improvements as required.

·        Develop and execute risk management strategies and mitigation plans.

·        Confirm and apply quality control activities.

·        Manage the study budget(s).

·        Participate in the training and development of the clinical study team.

 

Job Requirements:

·        Bachelor’s and/or master’s degree (in Health Sciences preferred)

·        Previous Work Experience:

-     1-2 years’ experience as Clinical Trial Project Manager is ideal, or 4-5 years’ experience as a lead CRA/SCRA

-     Minimum 5 years’ experience with clinical trial conduct

-     Experience in managing or coordinating international multi-center trials is highly desired.

·        Advanced user of Microsoft Office Suite; experience with project management software is desired.

·        Ability to handle complex projects; flexibility in managing changing priorities; strategic problem solving and judgement skills.

·        Capable of managing multiple projects, timelines and responsibilities.

·        Excellent written and verbal communication skills in English.

·        Ability to work with minimal direction.

·        Initiative taking and team working attitude.

·        Knowledge of ICH/GCP guidelines and regulatory requirements.

·        A genuine interest in the field of clinical development.

·        Willingness to travel approx. 20% of the time, including domestic and international travel.

 

For more information, please do not hesitate to reach out to me directly!

 

wpenticost@barringtonjames.com

+44 1293 77 66 44

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