PRAHS

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2017-42443

2017-42443

Title 
Medical Director - Pharmacovigilance
Job Locations 
-
United Kingdom-Reading
United Kingdom
Germany
Germany-Berlin
Germany-Mannheim
Germany-Munich
Posted Date 
8/17/2017

More information about this job

Overview

We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.

Responsibilities

We are currently looking for a Medical Director – Pharmacovigilance ideally with a background in General Medicine / Internal Medicine for our Medical Affairs Department in Mannheim, Germany or Reading, UK.

 

Joining our Medical Affairs Department working in a fast-paced, client-focused global environment the Medical Director's specialist expertise is called upon throughout the entire lifecycle of a project and as such the Medical Director plays a pivotal role in our business and project teams.  Alongside Business Development the Medical Director is a key contributor in raising our business profile to ensure we are the preferred partner for our clients with support on their projects.

 

As well as sharing your vast medical expertise at investigator meetings, kick-off meetings, and client face-to-face meetings other responsibilities will include: 

  • Maintaining a strong consultative relationship with the client throughout the project lifecycle
  • Providing input into the creation of the protocol and other study-related documents
  • Participating in discussions with regulators, key opinion leaders, senior management and our clients
  • Delivering training to external project teams and PRA colleagues
  • Reviewing medical data on the indication, inclusion / exclusion criteria and other medical issues to ensure our overall project deliverables are achieved and patient safety priortitised
  • Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plans

Qualifications

You are:

An expert in your field with an affinity to lead and inspire.

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 the following:

  • A medical qualification with license to practise and board certification
  • Experience in the desired therapy area is essential, ideally with experience in phase II-III projects either in industry or as an Investigator
  • Experience writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal is preferable 

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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