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
Qualified Person
Limerick
Quality Specialist
Tipperary
R&D Director
Galway
Recruitment Consultant
Republic of Ireland
R&D Manager
Galway
Medical Device Director
Republic of Ireland
Project Engineer
Republic of Ireland
Senior Recruitment Consultant
Republic of Ireland
R&D Director
Galway
Chemical Engineer
Tipperary
Head of R&D
Galway
CQV Lead
Tipperary
Graduate Laboratory Technician
Republic of Ireland
Process Engineer
Limerick
Senior Manufacting Engineer
Republic of Ireland
Senior Recruitment Consultant
Republic of Ireland
Project Manager
Limerick
R&D Manager
Galway
R&D Engineer
Dublin
R&D Director
Galway
R&D Manager
Galway
QC Analyst
Meath
R&D Manager
Galway
Project Engineer
Tipperary
C&Q Lead
Tipperary
Responsible Person (RP)
Republic of Ireland
Trainer
Dublin
Project Engineer
Limerick
Senior Quality Engineer-Remote
Republic of Ireland
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

Senior Principal Statistician(Clinical Trials)


Reference:SCA013501 Location: Cork
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Biostatistician

Senior Principal Statistician(Clinical Trials)
Our client, a global pharma company, are continuing to grow their statistics team and are now hiring for a Senior Principal Statistician to join them. This is a permanent role with hybrid working. As Senior Principal Statistician you will work develops or assists in the development of clinical protocol designs, clinical plans, and data analysis plans in collaboration with physicians, clinical research scientists, and/or medical colleagues. You will be responsible for working with research associates and scientists to establish a reporting database and for analysing data for clinical studies.

Responsibilities:

  • Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study
  • Select statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created
  • Collaborate with data sciences in the planning and implementation of data quality assurance plans
  • Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected
  • Perform peer-review of work products from other statistical colleagues
  • Influence team members regarding appropriate research methods
  • Collaborate with team members to write reports and communicate results
  • Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings
  • Respond to regulatory queries and interact with regulators
  • Understand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor
  • Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training

Requirements:
  • Ph.D., or equivalent or, M.S. with experience
  • Statistics, Biostatistics, or equivalent of field study
  • Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etc
  • Interpersonal communication skills for effective customer consultation
  • Teamwork and leadership skills
  • Technical expertise and application with working knowledge of experimental design and statistical analysis
  • Business process expertise associated with critical activities (e.g., regulatory submissions)
For more information please contact Sinéad Cullen on +353879500821 or [email protected]