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Job Details

CRA I or CRA II

Company: Chiltern
Location: client based
Reference: 2018-24693
Closing Date: 01 Jan 19
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

We are currently looking for talented CRAs to join our team in Israel. You would be working within our Flexible Solutions department (EMEA FSPx Team) dedicated to one sponsor/client.

Requirements:

Job Overview

We are currently looking for talented CRAs  to join our team in Israel. You would be working within our Flexible Solutions department (EMEA FSPx Team) dedicated to one sponsor/client.

Would you like to work for one of the best known big pharma companies? Our sponsor is a global mid sized pharma company with high working standards. Are you passionate about growing in Clinical Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.

You will become a part of our team who is always ready to help. You will have a possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

Our sponsor invests heavily in training and crafts modern system of Clinical Trials so if you are passionate about working with an outstanding team and expand your horizons feel free to reach us

Education / Qualifications

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

Experience

  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • Excellent understanding of Serious Adverse Event (SAE) reporting
  • Ability to resolve project-related problems and prioritize workload for self and team
  • You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).

Apply for this job: CRA I or CRA II

Contact Information:

Address:  London, UK
Covance Clinical and Periapproval Services Ltd Osprey House Maidenhead Office Park Westacott Way Maidenhead
SL6 3QH
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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