PRAHS

Returning Candidate?

2018-44543

2018-44543

Title 
Site Staff Training Lead - Home Based
Job Locations 
-
US-Remote
Posted Date 
1/8/2018

More information about this job

Overview

Do you want to watch clinical development change, or do you want to be the one to shape it?

 

 

Because we’re hoping you’re here for the latter.

 

 

Who are we?

We Are PRA.

 

We are 13,000+ employees strong, operating in more than 80 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.

 

Who are you?

You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

 

Still here? Good. Because if this is you, we’d really like to meet you.

 

 

Responsibilities

 

What will you be doing?

 

The In House Clinical Research Associate (IHCRA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements.  At the Senior level, the IHCRA will manage and lead all activities listed above and will ensure that all activities meet Sponsor and PRA expectations and are delivered in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.

 

  • Demonstrates good working knowledge of PRA systems and work environment
  • Demonstrates thorough knowledge of clinical research industry standards, practices, and regulations.
  • Exhibits good decision making skills utilizing all available resources for determining positive outcomes.
  • Successfully interacts with both internal and external customers, representing the organization on specific projects.

Qualifications

What do you need to have?

  • Minimum of 2 years of related experience

  • 4 year degree preferred
  • Experience with PC-Windows, word processing, and electronic spreadsheets required.
  • Knowledge of ICH and local regulatory authority drug research and development regulations required.
  • Clinical trials support or pharmaceutical industry experience required.
  • Experience leading a team in a clinical research environment preferred.





PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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