PRAHS

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2017-44287

2017-44287

Title 
Senior Clinical Trial Disclosure Associate
Job Locations 
-
United Kingdom
Posted Date 
12/15/2017

More information about this job

Overview

Senior Clinical Trial Disclosure Associate

Home based or office based Reading / London, UK

 

Commitment to our staff is only surpassed by our commitment to advancing treatment options available to patients. We understand the importance of supporting and investing in our people.

 

With 20% of our employees promoted last year, we don’t need to tell you that your career will thrive at PRA. We know it. And we can prove it. As we grow, so will you. Join us and Discover Your PRA.

 

As a Clinical Trial Disclosure Associate, 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 Clinical Trial Disclosure Associate is the subject matter expert for the public disclosure of clinical trials. Working as part of a global team you will execute registration and results disclosure activities in accordance with sponsor requirements and international regulations. Responsibilities of the role include:

 

  • Evaluation of clinical trial protocols to develop overall disclosure decision guidance.
  • Prepares disclosure requirements based on country disclosure regulations and sponsor policy.
  • Submissions of registration/results disclosures and updates throughout the study.
  • Consulting with government agencies to resolve submission queries.
  • Audits publicly disclosed information to ensure information is updated appropriately and is in compliance with applicable regulations.
  • Participates in internal and external disclosure committees to develop strategy, best practices and methodologies to clinical trial disclosure and to align with industry standards.

Qualifications

You are:

 

Proactive and time efficient with keen eye for detail.

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:

  • Proven experience of clinical trial registration/results disclosure with an in-depth knowledge to interpret disclosure activities.
  • A relevant degree ideally in life sciences and/or in-depth knowledge of scientific methodology and applicable regulations.
  • Ideally previously coordinated registration/results disclosure submissions.

 

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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