Precision Medicine Group
CRO
ClinicalResearchAssociate
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“Clinical Research Associate at Precision Medicine Group. Skills: Clinical study monitoring, Regulatory compliance, Site management. Monitor and own the progress of clinical studies at investigative sites. Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards”
Industry & Context.
Identify potential study risks; Propose solutions on how to mitigate them; Overcoming difficulties
Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
What They're Looking For.
Must Have
University degree life science/ pharmacy/ other health related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional, At least 6 months of experience as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies, Oncology experience, CRA Certification holder, Fluency in English and Italian
Nice to Have
Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
What You'll Do.
Monitor and own the progress of clinical studies at investigative sites
Ensure that clinical studies are conducted
and reported per protocol
and all applicable regulations and standards
Coordinate all necessary activities required to set up and monitor a study (i. e.
identify helping prepare regulatory submissions
conducting pre-study and initiation visits
How You'll Work.
Communication Scope
Project team updates
Full Job Description
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. Precision for Medicine is open to Clinical Research Associates I to join our team in Italy. This is a remote based position (homebased anywhere in Italy), with travel to sites for monitoring visits. About you: You are calm, thoughtful, and responsive when things don’t go as planned. You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game. You find quick and creative ways of overcoming difficulties. You have an impeccable eye for detail. You identify potential study risks and propose solutions on how to mitigate them. You take responsibility in the quality and outcomes of your work. You are adept at handling conflict by using tried and true resolution strategies. How we will keep you busy and support your growth: You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.). Qualifications: Minimum Required: University degree life science/ pharmacy/ other health related discipline or equivalent experi
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