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Clinical Research Associate I

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  • Company: Precision Medicine Group
  • Location: Italy
  • Work type: Remote
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  • Remote
  • Full Time
  • Italy (Remote)
  • Apply on company site

Precision Medicine Group — company details are preparing and update automatically in a few seconds (or refresh).

Precision Medicine Group is hiring a remote Clinical Research Associate I to join its clinical operations team in Italy, contributing to pioneering oncology and rare disease trials. If you want lower protocol loads, manageable travel, and a workplace where your perspective genuinely shapes outcomes, this role is built for you.

About the Role

This is a fully home-based Clinical Research Associate I position open to candidates located anywhere in Italy, with on-site monitoring visits to investigative sites. Precision Medicine Group is a CRO that does things differently: fewer concurrent protocols mean you can develop genuine protocol mastery, travel stays sensible, and your work-life balance holds steady. As a smaller organisation, we give CRAs real influence, hands-on support from direct line managers, and a culture reflected in retention rates well above the industry norm.

Key Responsibilities

  • Oversee and take ownership of clinical study progress at investigative sites across Italy.
  • Ensure trials are conducted, documented, and reported in line with the protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
  • Coordinate study set-up and monitoring activities, including identifying investigators and supporting regulatory submission preparation.
  • Carry out pre-study and site initiation visits as well as ongoing monitoring visits.
  • Spot potential study risks early and recommend practical mitigation strategies.

Qualifications

  • A university degree in life sciences, pharmacy, or another health-related field — or equivalent scientific/healthcare experience, or licensure as a healthcare professional.
  • A minimum of six months' experience as a CRA within a CRO, pharmaceutical, or biotech setting, or comparable relevant competencies.
  • Oncology experience and CRA Certification.
  • Availability for domestic travel with overnight stays, amounting to roughly 50–60% of your time.
  • Fluency in both English and Italian.
  • Preferred: a graduate or postgraduate qualification concentrated in a scientific or healthcare discipline.

About Precision Medicine Group

Precision Medicine Group advances the science of precision medicine by uniting innovative clinical trial designs, leading operational and medical specialists, advanced biomarker and data analytics, and a deep commitment to oncology and rare diseases. By linking specific tumour mutations to targeted treatments and pairing rigorous science with rich data, the company helps deliver insights that sharpen real-time decisions across the oncology development pathway.

How to Apply

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Listing facts

  • Role Clinical Research Associate I
  • Employer Precision Medicine Group
  • Location Italy · Remote-friendly
  • Type Full Time
  • Posted June 20, 2026
  • Apply by July 21, 2026
  • Country Italy
  • Overview Full job description on this page (401 words)

Facts above come from this job record on Get A Job.AI — not copied from third-party review sites.

Typical work in Clinical Research Associate

Independent occupational context from O*NET (U.S. public-domain labor data). This is about the occupation, not a rewrite of this employer's posting.

  • Conduct chemical analysis of body fluids, including blood, urine, or spinal fluid, to determine presence of normal or abnormal components.
  • Analyze laboratory findings to check the accuracy of the results.
  • Operate, calibrate, or maintain equipment used in quantitative or qualitative analysis, such as spectrophotometers, calorimeters, flame photometers, or computer-controlled analyzers.
  • Collect and study blood samples to determine the number of cells, their morphology, or their blood group, blood type, or compatibility for transfusion purposes, using microscopic techniques.
  • Enter data from analysis of medical tests or clinical results into computer for storage.
  • Establish or monitor quality assurance programs or activities to ensure the accuracy of laboratory results.

Source: O*NET

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precisionmedicine.com

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Clinical Research Associate I Precision Medicine Group · Italy