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Job Details

Clinical Research Associate/ CRA (UK) Home Based

Company: ICON Plc
Location:
Reference: CRA UK
Closing Date: 23 Nov 17
Type: Full Time
Salary (£): On Application
Benefits: Competitive

Job Summary:

Award winning international CRO. ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

Requirements:

This is an exciting opportunity to work within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring adherence to applicable regulations and principles of ICH-GCP.  

  • Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.  You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested
  • Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects

Role Requirements  

  • With a University degree in medicine, science, or equivalent; you will have previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level).  You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data
  • Possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner.  You should be able to produce accurate work to tight deadlines within a pressurised environment. 
  • You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence
  • You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.  

What’s Next?

Following your application if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.

Why choose us?

We want to be the Clinical Research Organisation that drives more client projects to market or accelerated decision than anyone else in the industry.  In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it.  Improving the lifestyle and well-being of our employee’s is central to our mission.  At ICON we encourage an environment to promote a healthy lifestyle and good work/ life balance with home based working and flexible schedules.

If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

http://careers.iconplc.com/

 

Apply for this job: Clinical Research Associate/ CRA (UK) Home Based

Contact Information:

Address:  Head Office
South County Business Park Leopardstown, Dublin 18
D18 X5R3
Rep. Ireland
Tel:  +353 1 291 2000
Website:  Visit Our Web Site

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