Clinical Research Associate I

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Occupation tasks (O*NET)

Public-domain labor data — prepare examples for 2–3 of these.

• 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.
• Analyze samples of biological material for chemical content or reaction.
• Set up, clean, and maintain laboratory equipment.

O*NET source

Company facts (cached)

Website: precisionmedicine.com

Public cache only — not an employee review.

Role overview (listing rewrite)

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…

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Questions to ask them

• What does success look like in the first 90 days for this role?
• How is the team structured, and who would I work with most?
• What tools and systems does this role use daily?
• Is the work primarily based in Italy, hybrid, or fully remote?