PRAHS

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2017-41153

2017-41153

Title 
TMF Specialist
Job Locations 
-
United Kingdom
Switzerland
Posted Date 
9/19/2017

More information about this job

Overview

TMF Specialist

London or Zurich

 

Who we are

 

PRA Health Sciences is an award winning CRO.

 

We are proud to have won Pharma Times 'Clinical Research Company of the Year' in 2017 for the fourth consecutive year. We aren’t winning these awards by chance; PRA is being recognised industry-wide for our dedication to the future of clinical development. Most importantly for you, at PRA we recognise that our success is down to our people.

 

As a TMF Specialist, you will be dedicated to one of our pharmaceutical clients with a truly global presence; this unique industry-changing partnership redefines collaboration. The program is ideal for individuals who thrive in a continually-evolving culture that mirrors PRA’s commitment to career development.

 

Responsibilities

Position overview

 

The TMF Specialist plays an integral role in our clients Global Clinical Services function supporting the trail management and operational activities of assigned clinical studies. We currently have an opening to join our team to supporting our clients vaccines portfolio. 

 

Role responsibilities include:

 

  • Support the activities associated with initiation, maintenance, and closure of clinical studies and individual investigative sites.
  • Ensure all trial operational activities are conducted in accordance with study timelines, company objectives and procedures.
  • Assist with the creation of the TMF plan.
  • Lead the implementation of the activities outlined in the TMF plan
  • Assist and/or lead investigator and internal reconciliation/ review of TMF.

 

Qualifications

You are

 

Analytical and conceptual with a high attention to detail, you should be able to communicate at a cross functional level demonstrating negotiation and persuasion skills.

Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

  • Experience in the pharmaceutical industry, supporting clinical study conduct in an operational or training capacity.
  • Basic knowledge of GCP and relevant regulations that govern essential documents
  • Preferably experience with clinical trial management systems
  • Ideally educated to degree level in a related scientific field

          

Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

 

PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

 

For more information please visit our website: www.prahs.com

 

 

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