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CRA- Grow Exponentially- The Netherlands/ Belgium

Business Type: Clinical Research Organisation
Job Type: Clinical Research Associate (CRA)
Job Level: Experienced (non manager)
Position: Full Time
Salary: EUR70000 - EUR75000 per annum + Standard Benefits
Location: Netherlands
Reference: 29968607
Closing Date: 30/10/21
Job Details:

A full-service science-driven, biotech-focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects.

Our extensive expertise can cover all phases of drug-related trials in all the therapeutic areas as well as clinical investigations for medical and diagnostic devices, Investigator Initiated Trials (IITs), and compassionate use programs.

Highly specialized professionals who can assist clients using deep know-how and experience to guarantee a top-quality level of Clinical Trial Management. Being a global full-service CRO, we can operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients'' challenging achievements.

No hiring Clinical Research Associate for those who have a scientific background, enjoy traveling throughout Belgium and/or The Netherlands, and are passionate about research.

Some of what you will do:

  • Collecting the documents required for the ethical and administrative submission
  • Checking the willingness to cooperate and the resources of the Investigator
  • Verifying the suitability of the site
  • Ensuring training and compliance with the protocol
  • Checking drug accountability and drugs delivery timeliness
  • Contacting sites to check the patient status, push enrollment, and manage queries in a timely manner
  • Ensuring the correct completion of informed consent
  • Checking adherence to inclusion/exclusion criteria
  • Checking that the enrollment schedule is in line with the study plan
  • Managing CRFs and internal reporting
  • Checking the completeness and consistency of collected data
  • Verifying that serious adverse events are reported according to Our company/Sponsor procedures
  • Handle study materials, including study drug(s), as foreseen for the specific study and as applicable
  • Promptly managing and follow-up protocol deviations
  • Participating in periodic meetings with Sponsors and Investigators
  • Maintaining a proactive relationship with the Data Center

Minimum Requirements:

  • Master''s Degree in scientific/healthcare-related subject
  • CRA certification
  • Willingness to travel
  • Good knowledge of English
  • Good planning, organization, and problem-solving abilities
  • Good communication and interpersonal skills

Receive a competitive salary with other benefits and the opportunity to develop your professional career with an expanding and growing company.

I am looking forward to speaking with you!

If this role is not quite right for you but you would like to have a conversation about other roles, please search and connect with me, Aleksandar Chernev, on LinkedIn.

We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We''re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting, for more information, to browse all our roles, or to let us know how we can help you.

Posted: 23/10/2021 | NPJ Ref: 286960
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