Clinical Research Associate II

Psi CRO; Lombardia; Hybrid; EUR 41,000 - 52,000; Full time

Job summary

Psi CRO in Milan offers a Hybrid role for a Clinical Research Associate II. You will conduct onsite and remote monitoring visits, perform CRF reviews, and manage site communications. You will identify sites, train less experienced CRAs, and work across sponsors in Italy with autonomy and ownership.

The role requires a Life Sciences degree, independent monitoring experience in Italy, and strong English proficiency. Travel and driver’s license are needed.

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.

Responsibilities

• 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.

Skills

On-site monitoring

Independent Italy monitoring

English proficiency

MS Office

Education

Life Sciences degree

Tools

MS Office

Job description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

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 rolein 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.

• 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

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.