PSI CRO

Global CRO delivering on-time patient enrollment

Clinical Research Associate 2

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeMilan, Metropolitan City of Milan, Italy

About the Job

Requirements

A college or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
Independent on-site monitoring experience in Italy.
Experience conducting all types of monitoring visits in Phase II and/or III.
Full working proficiency in English.
Proficiency in Microsoft Office applications.
Ability to plan, multitask, and work in a dynamic team environment.
Communication, collaboration, and problem-solving skills.
Ability to travel and a valid driver's license.

Responsibilities

Conduct and report all types of onsite and remote monitoring visits.
Perform case report form review, source document verification, and query resolution.
Manage site communications and site management activities.
Participate in the site identification process.
Assist in training less-experienced clinical research associates, depending on experience level.
Take the lead and ownership for assigned studies.
Work across multiple sponsors and broad therapeutic areas.
Work on fewer protocols to enable deeper study focus and stronger site relationships across Italy.
Work on complex clinical trials.

Job Description

We are looking for a Clinical Research Associate II to join a highly motivated, international team where collaboration, ownership, and trust are part of everyday work.

Hybrid role in Milan

You will:

Conduct and report all types of onsite monitoring visits as well as remote visits.
Perform CRF review, source document verification and query resolution.
Be responsible for site communication and management.
Be involved in site identification process.
Assist in training of less expert CRAs, depending on your level of experience.

What makes the role different:

You will use your managerial skills to take a lead for assigned studies, having true ownership rather than simply monitoring tasks.
You will work across multiple sponsors and broad therapeutic areas, keeping your work varied and scientifically engaging.
You will work on fewer protocols, enabling deeper study focus and stronger site relationships across Italy.
You will work on complex and scientifically interesting trials.
You will join a setup where CRAs are trusted with responsibility and autonomy.

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Italy
Experience in all types of monitoring visits in Phase II and/or III
Full working proficiency in English
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel and valid driver’s license

Additional Information

You will be part of an experienced, dynamic, and truly international team, where knowledge sharing and collaboration happen naturally across borders. Your contribution is visible, valued, and directly connected to study success.

Base salary range: €41.000 – €51.900 gross annual salary.
Actual compensation: The salary offered within the stated range will depend on objective, job-related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.
Additional compensation: bonus, incentive plans, and other benefits may apply.

About the Company

PSI CRO

Global CRO delivering on-time patient enrollment

PSI CRO is a global contract research organization that handles clinical trials for multiple therapeutic areas, with a focus on enrolling patients on schedule and delivering studies on time. Its services span feasibility assessments, trial planning, site selection, patient recruitment, and multi-continent trial execution across 50+ countries, backed by medical doctor resources dedicated to accurate timeline predictions. Unlike many CROs, PSI emphasizes predictable enrollment and on-time project delivery, aiming for high client satisfaction and repeat business through a pragmatic, no-nonsense approach. The company’s goal is to be regarded as the best CRO in the world by both clients and employees, achieved through reliable timelines, strong execution, and low staff turnover.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Switzerland
Founded: 1995

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