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Clinical Research Associate I - Unblinded Model

Labcorp Drug Development
Milan, Italy
Start date
2 Aug 2022
Closing date
31 Aug 2022

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Job Details

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Role Details:

We are recruiting for oursponsor-dedicatedbusiness inItalyand are currently seeking to hire anUnblinded Clinical Research Associate I ( already certified) with apermanent andfull-time contract.

Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.

At Labcorp Drug Development, you will have autonomy to organize your work and in return, you will be supported and empowered to go beyond the typical CRA role, to really be an expert on your protocols and to own your sites.

Responsibilities include but are not limited to:
  • Responsible for all aspects of unblinded study site monitoring including r outine visits and closing down sites;
  • Monitoring pharmacy sites to ensure GCP compliance across studies;
  • IMP management / accountability;
  • Ensuring the pharmacy staff are properly trained;
  • Checking prescriptions & chain of custody;
  • Involvement in audits.


We are searching for a university graduate with a life science degree or nursing background who relishes working in a fast paced environment, on complex and demanding protocols.

If you are someone who is eager to constantly develop and improve while working in a friendly and collaborative team environment; then we are looking forward to meeting you.
  • Minimum 6 months of clinical monitoring experience in international Pharma/CRO company preferred;
  • Experience in interventional studies preferred;
  • Excellent understanding of Serious Adverse Event (SAE) reporting;
  • Fluent in English.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement .


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.


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Maidenhead Office Park
Westacott Way
Littlewick Green
United Kingdom
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