Clinical Research Associate: Study Monitor & Site Liaison

OPIS s.r.l.; Desio; In loco; EUR 30.000 - 40.000; Tempo pieno

Descrizione del lavoro

A biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams, and managing study materials. This role offers a competitive salary and professional growth opportunities within a supportive environment.

Servizi

Competitive salary

Career development opportunities

Bonuses and additional benefits

Competenze

• 0-12 months of experience as CRA.
• Able to work independently under the supervision of others.
• Able to interact with personnel of clinical studies and investigations.

Mansioni

• Coordinate and oversee execution of clinical studies.
• Monitor sites to ensure compliance with protocols and regulations.
• Interact with regulatory teams and manage study materials.

Conoscenze

Knowledge of ICH-GCP

Good knowledge of Office Suite

Good knowledge of English language

Formazione

Degree in a scientific field

Descrizione del lavoro

A biotech-focused CRO in Italy is seeking a Clinical Research Associate (CRA) to coordinate and oversee clinical studies, ensuring compliance with protocols and regulations. The ideal candidate should have a degree in a scientific field and up to 12 months of experience as a CRA. Responsibilities include site monitoring, interaction with regulatory teams, and managing study materials. This role offers a competitive salary and professional growth opportunities within a supportive environment.