close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Clinical Trial Capabilities Assistant - Native Hebrew


Reference:POR/011615AS Location: Cork
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Clinical Research Associate

The role requires Native Hebrew & Fluent English, and requires relocation to Cork, Ireland.


A Hebrew speaking Trial Capabilities Assistantis required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives.

The role

The Trial Capabilities Assistant role provides technical support to the clinical trial capabilities team in support of clinical development. The assistant is responsible for activities related to investigator sites readiness, maintenance and close out.The assistant will ensure inspection readiness through a complete, accurate and readily available Trial Master File.

    • Initiate investigator site activities, including collection and submission of regulatory documents.
    • Track and ensure site compliance to effectively drive timelines aligned with company priorities
    • Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out
    • Support TPO and investigator payments as appropriate
    • Manage site account requests
    • Invoice query resolutions
    • Identify, communicate, and resolve issues
    • Accountable for accurate and complete data entry of clinical trial information into various clinical trial systems to allow tracking, performance metrics reporting and to meet regulatory compliance requirements.
    • Ensure inspection readiness through a complete, accurate and readily available Trial Master File
The Person
    • A degree or equivalent preferably in a scientific or health related field,
    • Two years clinical research experience or relevant experience preferred
    • Native Hebrew and Fluent English
    • Applied knowledge of project management processes and skills
    • Effective communication, team work and problem solving skills
    • Very good attention to details and accuracy

For further details please contact; Paula O’Reilly on 00 353 (0)87 7094141 or send CV in confidence to paula.oreilly@lifescience.ie