Overview

Reference Number: JO-2305-516900
Clinical Research Associate
Rate: Negotiable
Job Type: Permanent
Location: Milan

Clinical Research Associate – Italy

  • Italy based
  • Hybrid mainly home based, with targeted monthly visits to sites.
  • Attractive salary and great benefits package

An exciting opportunity to join 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. Who’s 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.

Key responsibilities shall include:

  • 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 enrolment, and manage queries in a timely manner
  • Ensuring the correct completion of informed consent
  • Checking adherence to inclusion/exclusion criteria
  • Checking that the enrolment 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 procedures
  • Handle study materials, including study drug(s), as foreseen for the specific study and as applicable
  • Promptly managing and follow-up protocol deviations
  • Maintaining a proactive relationship with the Data Centre

Key experience for the successful applicant:

  • 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

For more details and to discuss the opportunity in more detail please either drop me a LinkedIn message, email Danielle.holt@cpl.com or call at 0118 995 2206.

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