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CRA Sponsor dedicated in Belgium / Home-Based or office based positions

Employer
Labcorp
Location
Belgium
Salary
Competitive
Start date
29 Mar 2019
Closing date
24 Apr 2019

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Discipline
Clinical Research, Clinical Services
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Covance are currently looking for a talented Clinical Research Associates to join Covance in Belgium! This is a Sponsor dedicated position which will give you the opportunity to work with and for one of the most innovative pharmaceutical company in the industry. 

You will be part of a great and dynamic team, with the possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

Location: Brussels / Home-Based possible with presence required in client offices on a regular basis

This is time to join our EMEA FSPx Team! 

Responsibilities:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policy
  • Prepare accurate and timely trip reports
  • Responsible for all aspects of registry management as prescribed in the project plans
  • Undertake feasibility work when requested
  • Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor
  • Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
  • Assist with training, mentoring, and development of new employees, e.g. co-monitoring
  • Perform other duties as assigned by management

Requirements:

University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)

In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered

Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements

Thorough knowledge of monitoring procedures

Basic understanding of the clinical trial process

As a Covance CRA you will be able to enjoy the benefits of working for a company that values a WORK / LIFE BALANCE.

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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