Clinical Research Associate

JR Italy; Trentino-Alto Adige; In loco; EUR 35.000 - 65.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking skilled Clinical Research Associates (CRAs) to support a global study. This role involves ensuring timely and quality site monitoring activities in line with the Site Monitoring Plan. Ideal candidates will have a background in clinical research organizations (CRO) and possess strong communication skills, multitasking abilities, and a solid understanding of ICH GCP and clinical trial regulations. Join a rapidly expanding team that values quality and adherence to timelines, contributing significantly to project success in the biotech and pharmaceutical sectors.

Competenze

• 1-4 years of experience in clinical research site monitoring.
• Strong understanding of clinical trial regulations and ICH GCP.

Mansioni

• Ensure timely and quality site monitoring activities.
• Manage sites according to the Site Monitoring Master Plan.

Conoscenze

Site Monitoring

Communication Skills

Multitasking

Understanding of ICH GCP

Formazione

Bachelor’s in a scientific discipline

Master’s in a scientific discipline

Descrizione del lavoro

Social network you want to login/join with:

Client:

CliniRx

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

6891048445432299520337158

Job Views:

2

Posted:

02.05.2025

Expiry Date:

Job Description:

CliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer permanent opportunities on a global study basis. Ideal candidates will have a CRO background with experience across multiple therapeutic areas.

As a global CRO, we provide diverse clinical development and resource solutions, supporting biotech and pharmaceutical companies worldwide, with offices in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose:

Seeking skilled CRAs to ensure timely and quality site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure quality and timeliness.
• Site Management Compliance: Manage sites according to the SMMP and regulations to minimize QA audit observations.
• Site Identification: Assist in identifying new potential sites across therapeutic areas.
• Continuous Skill Development: Regularly improve technical and soft skills to enhance performance.

Work Relations:

• Report to the Manager of Clinical Operations.
• Collaborate with site monitoring team, site personnel, HR, site leads, and admin staff.

Value Added:

Your adherence to quality and timelines is crucial for project success.

Key Success Factors:

• High-quality, timely site monitoring activities.
• Prompt reporting to stakeholders.
• Education: Bachelor’s or Master’s in a scientific discipline.
• Experience: 1-4 years in clinical research site monitoring.
• Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication; multitasking ability under demanding timelines.