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Clinical Trial Specialist

Employer
Thornshaw Recruitment
Location
Dublin (County), Leinster (IE)
Salary
Unavailable
Start date
22 Feb 2019
Closing date
11 Mar 2019

Job Details

On behalf of my client, a Clinical Trial Organisation, we are actively seeking a Clinical Trials Assistant to join the team. 


This role is focused on providing clinical expertise to the delivery of projects.  The Clinical Trial Specialist (CTS) will typically work within a multifunctional team to deliver projects and will be responsible for the clinical accuracy of each project. They are also responsible for assisting in the definition stage of projects. 
The ability to communicate effectively with sponsors and explain clinical information to the project team is paramount to the successful completion of the role.

Key Responsibilities:

• Attend (chair if requested) internal team meetings throughout each project
• Attend and actively participate in client meetings
• Analysis of all documentation (protocol, manuals, etc.) for each project to determine critical points to be included in the training and supporting tools.
• Provide a detailed handover to the Instructional Designer and other team members to enable them to develop the content for the modules and tools
• Technical review of all content created by the team
• Responsible for the technical accuracy of all content
• Review and implementation of client comments
• Provide continuous clinical support to the team 
• Act as main point of contact for all clinical queries
• Work with Project Manager and Operations team to ensure that projects are completed according to agreed specifications 
• Prepare and complete a specification document for Patient Scheduling tool for each project
• Creation and review of department documentation and SOPs as needed


MINIMUM REQUIREMENTS
Knowledge 
• Aware of professional/clinical trial industry standards, excellent knowledge of ICH GCP required

Skills 
• Excellent attention to detail
• Excellent communicator and presenter
• Analytical thinker
• Proven ability to work well under stress/pressure for delivery
• Strong decision-making ability
• Strong team player 
• Ability to actively resolve issues that arise during the project

Experience 
• Minimum of 2 years in the clinical trial industry preferably in a CRA, data management, or medical writing position 
• BSc (Life Sciences) or RGN preferred 
• Knowledge of clinical trial services (eCRFs, IXRS, Central Laboratory, etc.) an advantage

For further details contact Tina at +353 1 2784671 or email your CV in confidence to tdunne@thornshaw.com

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

thornshaw-ourmission

For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
Website

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