Clinical Research Associate I

2 mesi fa

Milano, Italia Fortrea - Organic A tempo pieno

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Role Details:
We are recruiting for our sponsor-dedicated business in Italy and are currently seeking to hire an Unblinded Clinical Research Associate I ( already certified) with a permanent and full-time contract.

Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.

At Fortrea, you will have autonomy to organize your work and in return, you will be supported and empowered to go beyond the typical CRA role, to really be an expert on your protocols and to own your sites.

Responsibilities include but are not limited to:
- Responsible for all aspects of unblinded study site monitoring including routine visits and closing down sites;- Monitoring pharmacy sites to ensure GCP compliance across studies;- IMP management / accountability;- Ensuring the pharmacy staff are properly trained;- Checking prescriptions & chain of custody;- Involvement in audits.

**Requirements**:
We are searching for a university graduate with a life science degree or nursing background who relishes working in a fast paced environment, on complex and demanding protocols.

If you are someone who is eager to constantly develop and improve while working in a friendly and collaborative team environment; then we are looking forward to meeting you.- Minimum 6 months of clinical monitoring experience in international Pharma/CRO company preferred;- Experience in interventional studies preferred;- Excellent understanding of Serious Adverse Event (SAE) reporting;- Fluent in English.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit


Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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