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Clinical Trials Specialist

Employer
Thornshaw Recruitment
Location
Limerick (County), Munster (IE)
Salary
Negotiable Depending On Experience
Start date
7 May 2021
Closing date
6 Jun 2021

Job Details

On behalf of my client I am currently recruiting for a Clinical Trials Specialist for a full time, permanent position.

Job Description:

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.

Essential Position Functions:

• 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:

• 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

• Aware of professional/clinical trial industry standards, in particular excellent knowledge of ICH GCP required

For full details contact cnugent@thornshaw.com or call Ciara at 01 278 4702

Thornshaw Scientific is a division of the CPL group.  www.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

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

 

Company info
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