I'm looking for...
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
Contact Info
Sinead Cullen
Life Science

01 507 9252
[email protected]
Connect with me on
Project Engineer
Limerick
Project Manager
Limerick
R&D Manager
Galway
Senior CSV Specialist- Hybrid
Republic of Ireland
Quality Specialist
Tipperary
R&D Manager
Galway
Project Engineer
Limerick
Project Engineer
Tipperary
C&Q Engineer
Dublin
Head of R&D
Galway
Production Team Lead
Dublin South
Project Engineer
Limerick
CAD Technician
Republic of Ireland
Project Engineer
Limerick
R&D Engineer
Dublin
R&D Engineer
Galway
R&D Engineer
Limerick City
R&D Engineer
Galway
Quality Engineer
Limerick
Regulatory Affairs Specialist
Republic of Ireland
CSV Engineer
Limerick
Controls Engineer
Dublin South
QC Leader
Cork
Project Manager
Limerick
Quality Engineer
Limerick
Project Engineer
Republic of Ireland
R&D Manager
Galway
Engineering Technician
Dublin South
Medical Device Director
Republic of Ireland
Senior R&D Clinical Engineer
Republic of Ireland
VP Clinical Development
Republic of Ireland
Process Engineer
Limerick
CQV Lead
Tipperary
Senior R&D Engineer
Limerick City
GCP Inspector
Dublin
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 [email protected]
Details

Clinical Trial Design Site Training Associate


Reference:SCA011987 Location: Cork
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Clinical Trial Design Site Training Associate
Our client, a global pharma organisation, are currently recruiting for a Clinical Trial Design Site Training Associateto join their global centre of excellence for clinical trials on a permanent basis. The ideal candidate will be experienced in clinical development and clinical trials cost forecasting. This is a hybrid working role. As ClinicalTrial Design Site Training Associate, you will provide technical, project and operational expertise to support the strategy for a variety of aspects within the clinical programs which may include site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback).

Responsibilities:

  • Support the established strategy for the assigned area(s) of focus of site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback)
  • Partner with the CTDC Consultant(s) and appropriate Clinical Design Delivery & Analytics (CDDA) functions to deliver that strategy from identification, to timeline development, pre-work and post deliverable follow up
  • Support the creation of the appropriate deliverables (e.g., training, educational materials) in partnership with the CTDC Consultant(s) as well as the functional content owners and/or vendors by communicating timelines, facilitating review meetings and distributing outputs to cross functional partners
  • Support internal systems and communication throughout the execution of the project strategies
  • Understand specific capabilities and access points to maintain key platforms and systems in support of the CTDC team based upon the assigned area(s) of focus
  • Upload and maintain eTMF records in compliance with the requirements
  • Work closely with CTDC team members to continue to evolve internal standards, processes, tools, and best practices
  • Demonstrate strong communication skills, both verbal and written, with external partners including clinical trial participants and health care professionals (HCPs)
  • Work with external contracting of vendors, patients and HCPs
  • Contribute to a team culture that is valued for strategic and technical leadership
  • Provide technical support to ensure that processes for the assigned area(s) of focus are well integrated within the appropriate CDDA functions
  • Support the delivery of right-sized strategies that can be successfully implemented in the clinical programs
Requirements
  • Bachelors Degree in scientific or health related field or equivalent
  • Minimum of 3-5 years experience in pharmaceutical industry
  • General understanding of trial/protocol design and how that impacts overall site experience
  • Proven ability to deliver to timelines
  • Excellent communication (written and verbal) skills with internal and external partners
  • Demonstrated organizational and critical thinking skills
  • Ability to lead and influence toward a common goal
  • Ability to leverage critical thinking and problem solving skills to both sustain strong relationships with key business partners and for the identification and delivery of process improvements and identify innovative process improvements
  • Ability to thrive in a highly collaborative team environment, both in person and through virtual connections
For more information please contact Sinéad Cullen on +353879500821 or [email protected]